Clinical Data Management Programmer I (SAS)

Job Locations IN-Bangalore
Posted Date 2 weeks ago(8/3/2022 1:54 AM)
# of Openings
Data Management


To carry out any required tasks relating to the technical and programming requirements of data management.


To assist with all technical and programming tasks for the data management of allocated projects.

            To annotate the master CRF.

            To assist with definition of clinical databases and set up/ testing of data entry screens.

            To set up electronic consistency checks when necessary.

            To assist with writing and testing of edit checks.

            To set up import of electronic data as required.

            To assist with set up systems for study processing.

            To prepare electronic data for export and prepare any documentation for return at study completion as requested.

            To report progress against schedules to Project Manager or Lead Clinical Data Manager as appropriate.

            To be aware of and to work to the standards appropriate to the study.

            To perform quality control checks on programming outputs.

            To give opinion on possible improvements to procedures and standards.

            To perform other reasonable tasks as requested by management.

            When necessary to assist as needed with programming tasks for reporting of allocated projects. To perform quality control checks on programming outputs.



            Qualified to minimally BSc, BA or equivalent, preferably in a numerate discipline

            Having relevant past experience, within the pharmaceutical industry.


Work Experience:

            A minimum of experience in a technical/programming role within the pharmaceutical industry (or placement as part of undergraduate studies) preferably within Clinical Data Management.



            PC skills, including good knowledge of programmer software languages (particularly SAS)

            Knowledge of industry standard systems e.g. Oracle Clinical, Clintrial etc

            Knowledge of EDC systems preferable e.g. Inform, Rave, eTrials etc

            Understanding of Clinical Data Management processes.

            Good organisational skills.

            Good communication skills (oral and written), good analytical skills.


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