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Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 employer and mid-level 3-5y role raise competition, but niche clinical SAS specialization reduces applicant density.
Clinical trial data programming is industry-specific, limiting cross-industry transferability.
Explicit 3-5y requirement plus mandatory clinical database programming and SAS enforces strict filtering.
Job Description
Structured overview of role & requirementsAbout This Role
Develop and review complex edit checks, patient profile listings, reports, preprocessing checks, and map datasets for validation based on clinical study requirements using tools like Cognos, SAS, J-Review, or equivalent.
Perform data management activities including discrepancy review, query generation and resolution, and maintain clinical data projects with focus on data quality and cost-effective integration.
Conduct edit check validation by creating test cases, writing test scripts, and carrying out database validation and UAT against specified CRF/ECRF guidelines.
Minimum Requirements
Qualifications: BE degree.
Work Experience Required: 3 to 5 years in Clinical Database Programming and Clinical Data Management.
Primary Skill: Clinical Database Programming (P1 level).
Secondary Skill: Clinical Data Management (P1 level).
Ideal Candidate Profile
Experienced individual contributor accustomed to working with peers and receiving moderate instruction, with limited client or management interaction.
Skilled in handling moderate complexity analysis and problem solving.
Able to work rotational shifts as required by the role.