Match Score
Against your primary resumeLogin to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 employer, mid-level experience band, and metro location increase applicant competition considerably.
Clinical-trials domain expertise (SAS, CDM processes) significantly limits transferability across industries.
Explicit 5–8 years requirement plus mandatory clinical database programming (SAS/J-Review) skills raise strictness.
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 study requirements using tools like Cognos, SAS, J-Review, or similar.
Perform clinical data management activities including discrepancy review, query generation and resolution, and managing clinical data management projects.
Create CRF Completion Guidelines, SAE reconciliation guidelines, identify protocol deviations, perform edit check validation by creating test cases, writing test scripts, and conducting database validation (UAT).
Minimum Requirements
5 to 8 years of work experience.
Bachelor of Engineering (BE) degree required.
Mandatory skills: Clinical Database Programming and Clinical Data Management at proficiency level P1.
Role may require working in rotational shifts.
Ideal Candidate Profile
Experienced in handling complex problem analysis and solving within clinical data services and management domain.
Capable of working with minimal instruction and responsible for decisions impacting own and others' work.
Comfortable with some client interactions and potentially leading or overseeing small teams or work efforts.