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Tier-1 employer and metro location increase applicant interest, but clinical trial domain narrows candidate pool.
Role requires domain-specific clinical trial and biopharma data management experience, limiting cross-industry transferability.
Explicit degree-and-years alternatives plus clinical trial and vendor management requirements create moderate filtering.
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Accountable for end-to-end management and oversight of study/program data, ensuring high-quality, timely, decision-ready data for clinical trial delivery.
Lead development and execution of Data Management and Integrated Data Review Plans aligned with protocol and program strategy.
Drive database build, user acceptance testing, study conduct activities, data monitoring, and resolution of data metrics issues to ensure on-time study delivery and quality outputs.
Minimum education and experience combinations include: Doctorate OR Master’s + 2 years OR Bachelor’s + 4 years OR Associate’s + 8 years OR High school/GED + 10 years in life sciences, computer science, or business administration.
At least 5 years’ experience in life sciences or medically related field; 3 years in biopharmaceutical clinical research with biotech, pharmaceutical, or CROs preferred.
Experience managing cross-geography clinical trial teams and external vendors (e.g., CROs, labs, imaging).
Work Experience Required: Minimum 5 years in related fields with clinical trial experience as specified.
Experienced in global clinical trial data management with ability to lead cross-functional and cross-geographic teams.
Demonstrated capability in vendor management and coordination for clinical trial data activities.
Proven track record of accountability for data quality, delivery readiness, and driving resolution of data-related issues in clinical studies.