Looking for an exciting opportunity to advance your career in statistical programming? Look no further than Quanticate, the world-leading data-focused CRO. This role can be Hybrid, Remote or fully office based depending on your preference in the UK or Poland.    As a key member of our team, you will work alongside top global pharmaceutical companies and small biotechs to provide high-level statistical programming support for their clinical trials. You will use your technical expertise to deliver high-quality programming deliverables and documentation, adhering to current Quanticate and client-specific standard operating procedures (SOPs) and processes, as well as regulatory requirements and guidelines.   At Quanticate, we strongly believe in career development, providing you with membership to professional societies and encouraging your involvement in their activities and committees. We'll work with you to build the career you want, developing your skills and working on challenging problems to ultimately develop clinical therapies that matter.   As an ideal candidate, you should have a degree in a numerate discipline, a good understanding of basic statistics, and programming experience covering activities from study set-up to final reporting. You should also possess excellent analytical and organizational skills, strong communication skills, and a continuous improvement mentality with a good attention to detail. Candidates need to be already based in UK or Poland.    In return, we offer competitive salaries, flexible working arrangements, excellent benefits packages, and access to tools and computing systems including both SAS and R. At Quanticate, our people are our focus, and we understand that they are the key to our success. So, if you're looking for a challenging and rewarding career in statistical programming, join us at Quanticate!

Senior Programmer - Home based or Hybrid   About the Company: Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives: - Technical expertise in support of project deliveries and training development of Programming personnel. - Provide project and technical support, or line management support in the preparation and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Procedures: Core - Deliver excellent customer care in support of genuine value and a great customer experience. - Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. - Good knowledge of pharmaceutical industry standards - Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Provide mentoring in area of technical expertise. - Ability to work with different, functions, and across sites, as required. - Ability to review clinical documents, e.g. protocol, CRF and SAP. - Demonstrated SAS programming knowledge to an advanced level with expected results in SAS competency test. - Provide programming expertise and support within the function on programming standards, processes and procedures. - Provide high quality deliverables and appropriate communication to the client within expected timelines and budget as directed by the Project Lead. - Ability to represent the Company at external conferences, forums and working groups from a clinical programming perspective. Key Contacts/Relationships (Internal & External) Internal - Has a close working relationship with Senior Programmers (all levels), Line Manager, HR and other functional staff. - May deputise for a Senior Programmer II. - Works closely with the project study teams (statisticians, clinicians, medical writers, project management) for the successful delivery of programming activities. External - Some interaction with clients to complete various programming activities. To fulfil this role, the Senior Programmer I may be required to be a key participant in project team meetings and be responsive on an ad hoc basis.   Person Specification Education: - Qualified to degree level or equivalent, preferably in a numerate discipline. - Understanding of basic statistics. Work Experience: - Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Preferably have programming experience covering activities from study set-up to final reporting. Skills: - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.

About the Company Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives: - Provide high quality statistical support to clients, which conforms to current Quanticate and client-specific standard operating procedures (SOPs) and processes, and to applicable regulatory requirements. - Act as a lead point of contact with clients and accountable for enhancing customer satisfaction Lead cross-function operational teams to ensure successful delivery of projects. Procedures: - Provide high quality statistical support to studies including design and analysis of studies, writing SAPs and selecting optimum statistical methods, statistical sections of study protocols, estimates of sample size, and statistical general consultancy including study design and conduct. - Work as operational lead, ensuring tasks are appropriately delegated to members of the project team in line with the requirements of the project plan. Lead cross-function operational teams to ensure successful delivery of projects. - Monitor the work of the project team, and coordinate project delivery on time and within budget. - Provide regulatory and submission support (PSUR, BB, DSMB, etc.)     Key Contacts/Relationships (Internal & External) Internal - Work closely with their line manager to review objectives, progress and development. - Work closely with Senior and Principal Project Delivery Managers, Portfolio Managers/Director/VP, the Senior VP of Portfolio Delivery and Head of Programming and Statistics PMO allocated project teams, Senior Programming and Statistics staff, Group Managers, Clinicians and Medical Writers for the successful delivery of statistical activities. - Work in Partnership with support functions including HR, Finance, IT and BD. - Lead Statisticians, Senior Statisticians and Programmers assigned to projects to coordinate successful delivery of the required deliverables.   External - Interact extensively with clients (including client PoC, statisticians, clinicians, medical writers, project managers) to lead the client relationship and successfully deliver statistical output, ensuring excellent customer care. - Represent the company at external conferences and forums   Person Specification Education: - Qualified minimally to MSc level in Statistics or equivalent. And/or: - Have relevant experience within the pharmaceutical industry or medical sector. - Understand the principles and procedures of statistics.   Skills: - Strong statistical skills enabling independent provision of statistical advice and document review across a broad range of statistical applications. - Good knowledge of SAS and experience with other statistical software. - Proven ability to lead projects / Strong analytical and problem-solving skills. - Significant experience in more than one study phase, with good understanding of all phases.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.   For an informal chat please contact stephanie.muscroft@quanticate.com or connect with me via LinkedIn.

These positions (3 Vacancies) offer a fantastic opportunity to join a dedicated Statistics department. As a Graduate Statistician, you will have the opportunity to further develop your clinical statistics knowledge as well as gain experience in multiple therapeutic areas.   This is an office based role, you will be expected to spend the first year with 5 days a week in office to aid in training. You will be following a development plan designed to give you the knowledge you need to excel within the company. Following your first year it would be a hybrid model with 2-3 days in the office.   You will gain exposure to a broad range of clinical trial studies, working across Phases I-IV in a wide variety of therapeutic areas. Working as part of local and global project teams, you will have the opportunity to work on high profile, global studies for major pharmaceutical clients.

Technical expertise in support of project deliveries and training development of Programming personnel. Provide project and technical support, or line management support in the preparation and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Ensure high levels of customer care are provided

About the Company Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives: - Provide high quality statistical support to clients, which conforms to current Quanticate and client-specific standard operating procedures (SOPs) and processes, and to applicable regulatory requirements. - Act as a lead point of contact with clients and accountable for enhancing customer satisfaction Lead cross-function operational teams to ensure successful delivery of projects. Procedures: - Provide high quality statistical support to studies including design and analysis of studies, writing SAPs and selecting optimum statistical methods, statistical sections of study protocols, estimates of sample size, and statistical general consultancy including study design and conduct. - Work as operational lead, ensuring tasks are appropriately delegated to members of the project team in line with the requirements of the project plan. Lead cross-function operational teams to ensure successful delivery of projects. - Monitor the work of the project team, and coordinate project delivery on time and within budget. - Provide regulatory and submission support (PSUR, BB, DSMB, etc.)     Key Contacts/Relationships (Internal & External) Internal - Work closely with their line manager to review objectives, progress and development. - Work closely with Senior and Principal Project Delivery Managers, Portfolio Managers/Director/VP, the Senior VP of Portfolio Delivery and Head of Programming and Statistics PMO allocated project teams, Senior Programming and Statistics staff, Group Managers, Clinicians and Medical Writers for the successful delivery of statistical activities. - Work in Partnership with support functions including HR, Finance, IT and BD. - Lead Statisticians, Senior Statisticians and Programmers assigned to projects to coordinate successful delivery of the required deliverables.   External - Interact extensively with clients (including client PoC, statisticians, clinicians, medical writers, project managers) to lead the client relationship and successfully deliver statistical output, ensuring excellent customer care. - Represent the company at external conferences and forums   Person Specification Education: - Qualified minimally to MSc level in Statistics or equivalent. And/or: - Have relevant experience within the pharmaceutical industry or medical sector. - Understand the principles and procedures of statistics.   Skills: - Strong statistical skills enabling independent provision of statistical advice and document review across a broad range of statistical applications. - Good knowledge of SAS and experience with other statistical software. - Proven ability to lead projects / Strong analytical and problem-solving skills. - Significant experience in more than one study phase, with good understanding of all phases.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.   For an informal chat please contact Andrew.Dixon@quanticate.com or connect with me via LinkedIn.

Principle Programmer   About the Company: Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives:   - Multi-discipline role, with focus on delivering: - Project leadership of assigned complex/multiple projects and/or - Line management of assigned personnel and/or - Technical oversight in support of Operations deliveries, projects, initiatives, and training development of Programming personnel. - Lead process improvement and knowledge-sharing within the function. - Provide advanced project and technical support in the preparation and review of high quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Input to the development of the Programming function and its staff, including encouraging and supporting commercial awareness. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Procedures: Core - Deliver outstanding customer care in support of genuine value and a great customer experience. - Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. - Comprehensive knowledge of pharmaceutical industry standards. - Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Ensure adherence to all relevant SOPs, guidelines and processes. - Maintain up-to-date knowledge of the external regulatory environment relating to programming, including ICH/GCP requirements, and provide advice and educate colleagues (and clients) on changes to regulatory requirements and/or other guidelines relating to programming. - Provide high quality deliverables and appropriate communication within expected timelines and budget. - Use acquired in-depth knowledge and broad expertise to create, update and enhance procedures and applicable SOPs within Programming. - Identify, develop and lead cross-functional initiatives promoting knowledge-sharing within Quanticate. - Provide mentoring and leadership, as required. - Ability to perform Peer Review or Final Inspections, locally or globally, as required. - Ability to critically review and provide comments on clinical documents, e.g. protocol, CRF and SAP. - Ability to represent the Company at external conferences and forums. - May become involved in industry initiatives and organisations (e.g. PhUSE Committees/Steering bodies). - Participate in meetings such as recruitment, business development, finance and audits from a clinical programming perspective. - Perform other reasonable tasks as requested by management. - Assist with the implementation of and follow appropriate Project Management procedures. - Input to the development of functional goals and objectives. - Take responsibility for a functional objective. - To be responsible and accountable for daily and accurate completion of timesheets. - To ensure that all direct reports are actively encouraged and reminded of the need for daily and accurate completion of timesheets and to closely monitor the completion metrics. Technical Ability   - SAS Programming knowledge and experience to enable oversight of programming teams. - Provide programming advice internally and externally on complex clinical projects. - Oversee the delivery of consistently high quality output in a timely manner. - Ability to identify departmental technical training requirements. - Oversee and/or develop/deliver SAS training and workshops and other related training sessions, as applicable. - Encourage the acquirement of SAS, industry trends, other appropriate programming expertise and standards within Programming. Project Management Ability   - Comprehensive knowledge of regulatory agency guidelines. - Ability to plan resource requirements and project timelines, and recognise project training needs, including multiple/complex projects. - Pro-actively address changing timelines, risks, priorities and resourcing requirements in line with appropriate issue escalation processes. - Ability to establish and enforce the appropriate standards for multiple projects. - Ability to monitor project progress. Line Management Role   - Responsible for the line management of up to six programmers. - Perform an active role in the development of direct reports and/or provide training, mentorship and support for programmers as necessary. - Approve the timesheets of direct reports and review the timesheet entries which impact functional Key Performance Indicators. - Supervision of direct reports through fortnightly or monthly meetings (as a minimum) and provision of day-to-day support on an informal ongoing basis, as required. - Perform annual and interim reviews in accordance with HR processes and SOPs for direct reports. - Implementation of all processes applicable to the role of a Line Manager. - Ensure awareness of billability and other Key Performance Indicator targets. - Responsible for monitoring team resource allocation - Have input to recruitment and retention of staff within Quanticate. Key Contacts/Relationships (Internal & External) Internal - Work closely with Project Delivery Managers, Portfolio Managers/Director/VP, the Senior VP Portfolio Management, Head of Programming, Head of Statistics, programming project teams, Data Managers and Medical Writers for the successful delivery of programming activities. - Work in Partnership with support functions including HR, Finance, IT and BD. External - Interacts extensively with the client to complete various programming activities. To fulfil this role, the Principal Programmer may be required to be a key participant and/or lead project team meetings.   Person Specification Education: - Qualified to degree level or equivalent, preferably in a numerate discipline. - Understanding of basic statistics. Work Experience: - Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Preferably have programming experience covering activities from study set-up to final reporting. Skills: - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.

Senior Programmer   About the Company: Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives: - Technical expertise in support of project deliveries and training development of Programming personnel. - Provide project and technical support, or line management support in the preparation and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Procedures: Core - Deliver excellent customer care in support of genuine value and a great customer experience. - Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. - Good knowledge of pharmaceutical industry standards - Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Provide mentoring in area of technical expertise. - Ability to work with different, functions, and across sites, as required. - Ability to review clinical documents, e.g. protocol, CRF and SAP. - Demonstrated SAS programming knowledge to an advanced level with expected results in SAS competency test. - Provide programming expertise and support within the function on programming standards, processes and procedures. - Provide high quality deliverables and appropriate communication to the client within expected timelines and budget as directed by the Project Lead. - Ability to represent the Company at external conferences, forums and working groups from a clinical programming perspective. Key Contacts/Relationships (Internal & External) Internal - Has a close working relationship with Senior Programmers (all levels), Line Manager, HR and other functional staff. - May deputise for a Senior Programmer II. - Works closely with the project study teams (statisticians, clinicians, medical writers, project management) for the successful delivery of programming activities. External - Some interaction with clients to complete various programming activities. To fulfil this role, the Senior Programmer I may be required to be a key participant in project team meetings and be responsive on an ad hoc basis.   Person Specification Education: - Qualified to degree level or equivalent, preferably in a numerate discipline. - Understanding of basic statistics. Work Experience: - Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Preferably have programming experience covering activities from study set-up to final reporting. Skills: - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.

    About the Job:  For this role we are looking for strong technical applicants with experience in SAS programming and SQL. Rather than clinical research projects this role will work across real world evidence projects. This role would suit experienced programmers who want to get experience in life sciences.    About the Organisation: Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotech’s that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Objectives: - Further development of knowledge of SAS and advanced SQL, good programming practices and numerous Real World Data (RWD) databases. - Ability to manage time and keep Client informed about project progress. - Ensure high levels of customer care are provided. - Review available resources to find required information - Use and manipulate data stored in SQL database. - Ability to understand and modify SAS macros. - Use longitudinal databases (Administrative medical and pharmacy claims databases, Electronic Medical Records). - Technical experience in handling large datasets. - Basic understanding of statistical models used in Outcomes Research (OR) - Ability to ask questions effectively. Procedures: Core - Undertake training as directed by line management and mentor. - Deliver excellent customer care in support of genuine value and a great customer experience. - Provide high quality deliverables and appropriate communication to the client within expected timelines. - Program tables, figures and listings and derived datasets according to the request description. - Perform quality control checks and complete quality control documentation for programming plans, specifications, outputs/derived datasets. - Perform other reasonable programming tasks as requested by management. - Demonstrate understanding of current Quanticate, and client-specific Standard Operating Procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Follow appropriate Project Management procedures. - Work to the appropriate standards of the project. - Communicate effectively with OR team. - Provide input to improvements to processes, procedures and standards. - Support the training and development of other programmers. - Mentor Graduate programmers - To be responsible and accountable for daily and accurate completion of timesheets.   Key Contacts/Relationships (Internal & External) Internal Work closely with the Programming Department, OR team members, mentor and line manager. External Interaction with Client Point of Contact (PoC) and limited interaction with Project Requestor/Statisticians/Data Scientists to complete various programming activities. Programmer II may be required to participate in project team meetings and be responsive on an ad hoc basis.   Person Specification - Qualified to degree level or equivalent, preferably in a numerate discipline. - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good knowledge of SQL, good organisational skills, good communication skills (oral and written), good analytical skills and attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.  

Lead Principal Programmer   About the Job:  For this role we are looking for strong technical applicants. Rather than leading projects this role will work across projects offering advice and support on the technical side whether that is resolving challenges or mentoring junior professionals on how to complete them. Though not a direct leadership role you will be mentoring staff. You will be supporting the Head of Programming on project delivery and will have great visibility in the company and with the CEO and COO.  This role would suit experienced programmers who want to stay 'hands on' rather than moving into management.    About the Organisation: Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotech’s that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives:   - Multi-discipline role, with focus on delivering: - Project leadership of assigned complex/multiple projects and/or - Line management of assigned personnel and/or - Technical oversight in support of Operations deliveries, projects, initiatives, and training development of Programming personnel. - Lead process improvement and knowledge-sharing within the function. - Provide advanced project and technical support in the preparation and review of high quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Input to the development of the Programming function and its staff, including encouraging and supporting commercial awareness. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Procedures: Core - Deliver outstanding customer care in support of genuine value and a great customer experience. - Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. - Comprehensive knowledge of pharmaceutical industry standards. - Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Ensure adherence to all relevant SOPs, guidelines and processes. - Maintain up-to-date knowledge of the external regulatory environment relating to programming, including ICH/GCP requirements, and provide advice and educate colleagues (and clients) on changes to regulatory requirements and/or other guidelines relating to programming. - Provide high quality deliverables and appropriate communication within expected timelines and budget. - Use acquired in-depth knowledge and broad expertise to create, update and enhance procedures and applicable SOPs within Programming. - Identify, develop and lead cross-functional initiatives promoting knowledge-sharing within Quanticate. - Provide mentoring and leadership, as required. - Ability to perform Peer Review or Final Inspections, locally or globally, as required. - Ability to critically review and provide comments on clinical documents, e.g. protocol, CRF and SAP. - Ability to represent the Company at external conferences and forums. - May become involved in industry initiatives and organisations (e.g. PhUSE Committees/Steering bodies). - Participate in meetings such as recruitment, business development, finance and audits from a clinical programming perspective. - Perform other reasonable tasks as requested by management. - Assist with the implementation of and follow appropriate Project Management procedures. - Input to the development of functional goals and objectives. - Take responsibility for a functional objective. - To be responsible and accountable for daily and accurate completion of timesheets. - To ensure that all direct reports are actively encouraged and reminded of the need for daily and accurate completion of timesheets and to closely monitor the completion metrics. Technical Ability   - SAS Programming knowledge and experience to enable oversight of programming teams. - Provide programming advice internally and externally on complex clinical projects. - Oversee the delivery of consistently high quality output in a timely manner. - Ability to identify departmental technical training requirements. - Oversee and/or develop/deliver SAS training and workshops and other related training sessions, as applicable. - Encourage the acquirement of SAS, industry trends, other appropriate programming expertise and standards within Programming. Project Management Ability   - Comprehensive knowledge of regulatory agency guidelines. - Ability to plan resource requirements and project timelines, and recognise project training needs, including multiple/complex projects. - Pro-actively address changing timelines, risks, priorities and resourcing requirements in line with appropriate issue escalation processes. - Ability to establish and enforce the appropriate standards for multiple projects. - Ability to monitor project progress. Line Management Role   - Perform an active role in the development of direct reports and/or provide training, mentorship and support for programmers as necessary. - Approve the timesheets of direct reports and review the timesheet entries which impact functional Key Performance Indicators. - Supervision of direct reports through fortnightly or monthly meetings (as a minimum) and provision of day-to-day support on an informal ongoing basis, as required. - Perform annual and interim reviews in accordance with HR processes and SOPs for direct reports. - Implementation of all processes applicable to the role of a Line Manager. - Ensure awareness of billability and other Key Performance Indicator targets. - Responsible for monitoring team resource allocation - Have input to recruitment and retention of staff within Quanticate. Key Contacts/Relationships (Internal & External) Internal - Work closely with Project Delivery Managers, Portfolio Managers/Director/VP, the Senior VP Portfolio Management, Head of Programming, Head of Statistics, programming project teams, Data Managers and Medical Writers for the successful delivery of programming activities. - Work in Partnership with support functions including HR, Finance, IT and BD. External - Interacts extensively with the client to complete various programming activities. To fulfil this role, the Principal Programmer may be required to be a key participant and/or lead project team meetings.   Person Specification Education: - Qualified to degree level or equivalent, preferably in a numerate discipline. - Understanding of basic statistics. Work Experience: - Very experienced SAS programmer within CRO/life sciences area. - Very good knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Programming experience covering activities from study set-up to final reporting. Skills: - Should have strong PC skills, very good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.  

Quanticate, one of the world's largest Clinical Research Organisation specialising in the provision of data-related services, is offering an exciting opportunity for three Graduate Statisticians to join our growing statistics department in our Manchester office.   As a Graduate Statistician, you will be working within our global statistics department, providing the highest quality statistical services to our pharmaceutical, biotechnology, nutritional and medical device clients. This is an office-based role, and you will be expected to spend the first year with 5 days a week in the office for training purposes, with a hybrid model of 2-3 days in the office following your first year.   You will have the opportunity to further develop your clinical statistics knowledge, as well as gain experience in multiple therapeutic areas. You will be following a development plan designed to give you the knowledge you need to excel within the company, with structured career paths across each of our functional areas, including Junior and Expert Academies that will fast-track you up the CRO career ladder.

Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Location: Bangalore/ Hyderabad (Office Based/Hybrid)

Quanticate, the Biostatistics and Data Experts are engaging with suitably experienced statistical programming professionals for the role of Principal Programmer. The permanent role will be instrumental in delivering Quanticate client services within the Clinical Trial, Research, Pharmaceuticals spaces.   Working at Quanticate offers a career with variety, exposure to clients, and an excellent culture of learning, development and career transformation. You will be part of an inclusive and diverse organisation that has adapted and innovated for over 28 years. Our senior level roles are key to the quality of our deliverables. They perform the direct validation of other programmers’ work and support, train, and mentor Quanticate juniors and peers alike. Initiatives such as the on-going delivery of R training powers our programmers with the tools and technical expertise to adapt to an ever-changing industry.     We offer remote working from anywhere in the United Kingdom with hybrid, flexible and on-site options. A warm welcome awaits you in our Manchester City and Hitchin - Hertfordshire locations.     Objective/Role mission statement - To deliver technical expertise in support of project deliveries, and the training and development of programming personnel. - To provide project and technical support, or line management support in the preparation and review of highquality programming deliverables and documentation, as well as the processes and standards required. - To provide best-in-class, high quality, efficient support that ensures delivery in line with Quanticate/client standard operating procedures (SOPs) and processes. - To ensure all applicable regulatory requirements are met and guidelines followed on behalf of the client and Quanticate.   What we’re looking for - Demonstratable SAS programming knowledge (R, SPSS, SQL, ADaMS would be beneficial) - Experience of clinical/pharmaceutical drug development and associated ICH/GCP guidelines - Experience reviewing clinical documents, e.g., Protocol, SDTM, eCRF, SA. - Good knowledge of pharmaceutical industry standards - Experience delivering SAS training/workshops and other programming-related training sessions   What we offer you - 25 days annual leave + bank holidays - Holiday purchase scheme - Fully remote +hybrid options - Rural and City locations including Hitchin, Manchester - Flexible working hours - Life Cover - Extensive training culture - Employee wellbeing support to all staff

Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Responsibilities - Provide project and technical support, or line management support in the preparation and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Ability to review clinical documents, e.g. protocol, CRF and SAP. - Ability to represent the Company at external conferences, forums and working groups from a clinical programming perspective. - Contribute to SAS training and workshops and other programming-related training sessions as applicable.   Skills & Qualifications - Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.   For an informal chat please contact lizzie.fitch@quanticate.com or connect with me via LinkedIn.

Senior Programmer   About the job: Quanticate is the world leading data-focussed CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming input. We need talented individuals to help us fulfil our customers’ needs.   Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical programme, to small biotechs that are taking their first steps in clinical development   We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.   Job Specification Objectives: - Technical expertise in support of project deliveries and training development of Programming personnel. - Provide project and technical support, or line management support in the preparation and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients. - Provide high quality, timely support that conforms to current Quanticate (or client-specific) standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Procedures: Core - Deliver excellent customer care in support of genuine value and a great customer experience. - Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. - Good knowledge of pharmaceutical industry standards - Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. - Provide mentoring in area of technical expertise. - Ability to work with different, functions, and across sites, as required. - Ability to review clinical documents, e.g. protocol, CRF and SAP. - Demonstrated SAS programming knowledge to an advanced level with expected results in SAS competency test. - Provide programming expertise and support within the function on programming standards, processes and procedures. - Provide high quality deliverables and appropriate communication to the client within expected timelines and budget as directed by the Project Lead. - Ability to represent the Company at external conferences, forums and working groups from a clinical programming perspective. Key Contacts/Relationships (Internal & External) Internal - Has a close working relationship with Senior Programmers (all levels), Line Manager, HR and other functional staff. - May deputise for a Senior Programmer II. - Works closely with the project study teams (statisticians, clinicians, medical writers, project management) for the successful delivery of programming activities. External - Some interaction with clients to complete various programming activities. To fulfil this role, the Senior Programmer I may be required to be a key participant in project team meetings and be responsive on an ad hoc basis.   Person Specification Education: - Qualified to degree level or equivalent, preferably in a numerate discipline. - Understanding of basic statistics. Work Experience: - Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. - Preferably have programming experience covering activities from study set-up to final reporting. Skills: - Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.   At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.