Associate Director, Clinical Research Scientist

A global, commercialized biopharmaceutical company in Middlesex County, MA is seeking an Associate Director, Clinical Research Scientist to join its Clinical Development organization. This role is ideal for a senior clinical scientist who thrives in cross‑functional environments and enjoys shaping clinical strategy across early and late‑phase development.

What You’ll Do

• Lead clinical data review activities to ensure high‑quality, decision‑ready datasets across assigned studies.
• Support DSMB activities, including preparation of materials and interpretation of outputs.
• Contribute to clinical study protocol development and ensure alignment with program objectives and regulatory expectations.
• Partner with cross‑functional teams to define endpoints, inclusion/exclusion criteria, and study methodologies.
• Oversee selection and validation of clinical outcome measures and data collection strategies.
• Conduct literature reviews to inform clinical trial design and development plans.
• Summarize and present clinical insights to internal teams and senior leadership.
• Contribute to clinical development plans spanning Phase 1–3 programs.
• Evaluate opportunities for new indications and support strategic program expansion.
• Provide scientific input into regulatory documents and support interactions with health authorities.
• Contribute to scientific publications, abstracts, and conference presentations.
• Build and maintain relationships with KOLs, investigators, and external experts.

What You Bring

• Advanced degree (PhD or PharmD) in related discipline.
• 5+ years of industry experience in clinical research within pharma/biotech.
• Demonstrated experience in clinical trial design and execution, and data interpretation.
• Experience in neuroscience, CNS disorders, pain, or psychiatry is highly desirable.
• Proven ability to lead clinical research initiatives and contribute to strategic development plans.
• Experience collaborating with investigators, KOLs, and external clinical experts.
• Solid understanding of ICH, GCP, and regulatory guidelines.
• Excellent communication skills and ability to operate effectively in a matrixed environment.