Back
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Tier-1 brand, metro location, and broad non-niche skillset increase applicant density.
Requires regulated clinical development, CDISC and validated systems experience, limiting cross-industry transferability.
Explicit 10+ years, regulated clinical experience and CDISC/validation requirements create high selection rigour.
Lead multiple analytical reporting teams to deliver clinical data reports, dashboards, and data-review solutions across Global Development.
Set and govern multi-year technology and capability roadmaps, balancing study-specific needs with reusable, scalable reporting solutions.
Partner cross-functionally and manage vendor delivery to ensure quality, compliance, and alignment with clinical development priorities.
Doctorate with 5+ years experience, or Master’s with 8+ years experience, or Bachelor’s with 10+ years experience relevant to clinical development analytics.
At least 2 years people-management or technical leadership experience in clinical development or related regulated environments.
Demonstrated delivery of clinical data reports, dashboards, or analytics in pharmaceutical, biotech, CRO or similar regulated settings.
Not explicitly mentioned in the JD: notice period, specific location, or mandatory programming languages, but experience with SQL/Python/SAS or visualization tools is preferred.
Experience leading global, matrixed teams focusing on clinical data and reporting technology in regulated environments.
Strong domain knowledge of clinical development workflows, EDC, CDISC standards, data governance, and regulated system validation.
Proven capability to drive cross-functional collaboration, capacity planning, quality metrics, and vendor management in analytical reporting.