Senior Analyst, Data Acquisition

Design, develop, validate, and maintain automated clinical data review and reporting solutions across multiple data sources.

Lead the implementation of clinical data checks, reconciliations, and review workflows ensuring compliance and quality in clinical trial data.

Provide technical oversight and mentorship on coding standards, solution architecture, and collaborate with cross-functional teams to meet study milestones and produce inspection-ready outputs.

Bachelor’s degree in Engineering, Life Sciences, Computer Sciences, Mathematics, Physics, or equivalent.

4+ years of experience in data acquisition or related clinical research/information systems roles.

Proven expertise with Veeva CDB, Veeva CDMS Reports, Domino, R, Python, SQL, and clinical data standards.

Deep understanding of clinical trial processes, data review methodologies, reconciliation processes, and regulatory requirements.

Experienced in leading complex technical initiatives and influencing cross-functional stakeholders in clinical data management or programming.

Strong technical skills combining clinical data review programming with advanced statistical/computational tools like R and Python.

Comfortable operating in regulated clinical trial environments requiring high quality, compliant, and scalable data review solutions.