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Tier-1 employer and Hyderabad metro increase competition, though role is specialized.
Requires biopharma clinical trial and CRO/vendor experience, limiting cross-industry transferability.
Explicit degree-plus-years options and required clinical trial experience indicate high filter strictness.
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Accountable for end-to-end management and oversight of clinical study/program data ensuring high-quality, timely, decision-ready data delivery.
Lead development and execution of Data Management Plan and Integrated Data Review Plan aligned to clinical protocol and strategy.
Drive study database build, UAT, go-live readiness, supervise data cleaning, query management, reconciliation, and database lock preparation to ensure delivery readiness.
Doctorate degree OR Master’s + 2 years OR Bachelor’s + 4 years OR Associate’s + 8 years OR High School + 10 years experience in life sciences, computer sciences, or business administration.
Preferred: 5 years’ experience in life sciences or medically related field with 3 years in biopharmaceutical clinical research on clinical trials within biotech, pharma or CRO.
Experience managing external vendors such as CROs, central labs, imaging vendors.
Work Experience Required: At least 5 years with clinical research experience as specified.
Experienced leader capable of single-point accountability for clinical study data quality, delivery, and cross-functional alignment across global teams.
Skilled in clinical trial data lifecycle including database build, user acceptance testing, study conduct metrics monitoring, and data deliverables management.
Experienced in collaborating with multiple geographies and managing external vendors to ensure timely clinical trial data delivery.