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Clinical Drug Analyst Jobs (NOW HIRING)

Rxadvance Corporation

Clinical Advisor

Southborough, MA · On-site

$100K - $110K/yr

Makes strategic recommendations including benefit design and formulary analysis, provision of clinical drug information, Pharmacy & Therapeutics support and participation, rational drug formulary ...

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Clinical Drug Analyst information

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How much do clinical drug analyst jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical drug analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

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Infographic showing various Clinical Drug Analyst job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Associate Director, Clinical Data Management

Princeton, NJ • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Life, Retirement, PTO

Posted 11 days ago

Job description

Position Summary

Associate Director, Clinical Data Management

Key Responsibilities
  • Provide clinical data management leadership for complex clinical development projects; align on and drive data collection requirements.
  • Plan, coordinate, and deliver complete, high-quality, reliable clinical trial data on time.
  • Lead end-to-end clinical data management; primary point of contact for internal/external study teams.
  • Set program-level data collection/review standards with cross-functional teams and global standards.
  • Oversee third-party vendors for data management deliverables; manage data currency.
  • Collaborate on EDC and related data collection systems (eCOA, External Data, Safety Gateway); enforce data standards and quality expectations.
  • Author/review DM study plans and documents (e.g., Data Quality Management Plan, Data Validation Plans, Data Review Plan, eCRF Completion Guidelines).
  • Chair Data Quality Review meetings to ensure data currency, quality, and completeness.
  • Represent DM on cross-functional project and submission teams; lead/support Health Authority inspections, audits, and CAPA.
  • Coach junior Data Management Leads; lead/co-chair department Data Management Lead forums.
Qualifications & Experience
  • Bachelor’s degree in life sciences/data science/statistics (advanced degree preferred).
  • 7+ years Biopharma/CRO experience; 3+ years in study/program leadership.
  • Travel: 5–10%.
Required/Preferred Skills
  • Clinical drug development process knowledge; FDA/ICH and data management best practices.
  • EDC systems expertise (Medidata RAVE preferred); strong MS Office skills.
  • Strong project management, metrics analysis/reporting; excellent oral/written communication.
  • Knowledge of submission requirements (e.g., NDA/BLA/MAA).
Benefits (as listed)
  • Health coverage; wellbeing support; financial wellbeing/protection (401(k), disability, life/accident, insurance, legal support).
  • Paid time off options (flexible time off and/or vacation per employee type) and other eligibility-based leaves.
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