Principal Clinical Data Reviewer/scientist

Biogen

Research Triangle Park, NC, United States
Base: $116,000.00-$155,000.00; bonus/equity: short...
Clinical trial data integrity
Data quality and plausibility assessment
Clinical data review tools
Lead clinical and scientific data review activities across assigned clinical studies, ensuring data accuracy, consistency, and alignment with protocol expectations and therapeutic objectives

Job Summary

  • Lead clinical and scientific data review activities across assigned clinical studies, ensuring data accuracy, consistency, and alignment with protocol expectations and therapeutic objectives.
  • Collaborate closely with cross‑functional teams, including Clinical Development, Biostatistics, Pharmacovigilance, and Study Operations, to drive data‑driven decision‑making and ensure high-quality trial execution.
  • The base compensation range for this role is: $116,000.00-$155,000.00; Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities; Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

Lead clinical and scientific data review activities across assigned clinical studies, ensuring data accuracy, consistency, and alignment with protocol expectations and therapeutic objectives.

Salary

Base: $116,000.00-$155,000.00; Bonus/Equity: Short term and long-term incentives, cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurances, Fitness & Wellness programs, Disability insurance, paid vacation, holidays, paid days off for Personal Significance, sick time, Maternity and Parental Leave, 401(k) with match, ESPP, tuition reimbursement

Skills & Requirements

Must-have

  • Clinical trial data integrity
  • Data quality and plausibility assessment
  • Clinical data review tools
  • Cross-functional team collaboration
  • Drug development knowledge
  • GCP, ICH E6(R2)/E6(R3) knowledge

Nice-to-have

  • Scientific data excellence passion
  • Actionable insights from complex data
  • Continuous improvement mindset
  • Agile team leadership
  • Vendor performance and quality mitigation

Key Requirements

  • 5+ years in Clinical Operations/Scientific role or DM
  • Medidata Rave experience required
  • Experience with eCRF, external data, integrated datasets
  • CDISC standards (SDTM, ADaM) familiarity
  • Bachelor’s degree in life sciences or related discipline

Work Rights

Not specified

Tailored Resume

Cover Letter