Senior Clinical Data Associate

Role Overview

The Senior Clinical Data Associate works in close partnership with Lead/Clinical Data Managers and supports multiple oncology studies with increased independence and accountability. The role contributes directly to data quality, timeline adherence, and inspection readiness while collaborating closely with Clinical Operations, Safety, Biostatistics, and external vendors.

What You Will Do

Perform end to end clinical data review activities, including query generation, review, follow up, and closure, in accordance with study specific guidelines and timelines. Conduct in house data review and provide detailed feedback to the Lead/Clinical Data Manager or CRO Data Management team.

Why It Might Be a Fit

The ideal candidate will have a solid understanding of clinical data management processes and clinical trial conduct under ICH/GCP, hands-on experience with EDC systems, query management, data cleaning, and reconciliation workflows, and strong attention to detail and ability to manage competing priorities across multiple studies.

Requirements

• Bachelor’s degree in life sciences or a related field
• Minimum 3 years of clinical data management experience in the pharmaceutical or biotech industry
• Oncology experience preferred

Benefits

• Base salary
• Merit-based salary increases
• Short incentive plan participation
• 401(k) plan
• Medical, dental, vision, life and disability insurances
• Leaves provided in line with your work state
• Flexible paid time off
• 11 paid holidays
• Additional time off for a shut-down period during the last week of December
• 80 hours of paid sick time upon hire and each year thereafter