Clinical Trial Physician, Neuroscience

3+ years

$243,930 – $295,589

Princeton Junction

10 Oct. 4, 2025

Job Description

Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🏷️ Job Title

Clinical Trial Physician – Neuroscience

📍 Location: Princeton, NJ, US (Hybrid)
🏢 Company: Bristol Myers Squibb (BMS)
🕒 Employment Type: Full-time
💰 Compensation: $243,930 – $295,589 (Princeton, NJ); up to $331,063 at other sites + incentive cash and stock opportunities

🧭 Position Overview

The Clinical Trial Physician provides medical oversight and accountability for clinical trials across Phases 1–4. This role is embedded within Clinical Development, a global organization responsible for clinical strategy, trial design, execution, and interpretation.

The physician partners with cross-functional teams to ensure the safety, efficacy, and scientific rigor of clinical trials while providing expert medical input on protocols, trial conduct, and regulatory submissions.

⚙️ Key Responsibilities

Medical Monitoring

Serve as a key member of the Study Delivery Team (SDT) and Clinical Development Team (CDT).
Review trial data, including eligibility assessments.
Collaborate with Clinical Scientists (CS) on site interactions, medical questions, and safety guidelines.
Assess key safety-related serious adverse events with Worldwide Patient Safety; oversee safety narratives.
Provide medical input on protocol development, including inclusion/exclusion criteria and safety-related considerations.
Ensure compliance with GCP and other regulatory requirements.

Clinical Development Expertise & Strategy

Collaborate with Clinical Development Leads to design clinical plans and protocols aligned with regulatory and disease strategy goals.
Provide oversight and medical accountability for multiple studies.
Analyze benefit/risk of protocols within matrix team structures.
Support executional delivery (site activation, enrollment tracking, adjudication of protocol deviations).
Build and maintain relationships with principal investigators and external thought leaders.
Maintain up-to-date knowledge of the disease area, treatment landscape, and competitive pipeline.
Deliver ongoing medical education to study teams, investigators, and other stakeholders.

Health Authority & Publications

Contribute to regulatory interactions and advisory board meetings.
Author clinical content for Clinical Study Reports (CSRs), regulatory reports, briefing books, and submission documents.

🎓 Qualifications & Experience

Education

MD or US-equivalent medical degree required.
Subspecialty training in the applicable therapeutic area is preferred.

Experience

Minimum 3 years of industry and/or clinical trials experience.
Strong understanding of the drug development process.
Expertise in clinical trial planning, protocol development, and medical monitoring.
Knowledge of statistical methods, hypothesis testing, and data interpretation.

Skills

Strong leadership and teamwork capabilities.
Excellent verbal and written communication in scientific and clinical settings.
Ability to maintain scientific reputation within the disease area.
Ability to travel domestically and internationally as needed.

🌍 Work Culture & Environment

Hybrid work model with flexibility in onsite/offsite attendance.
Operates within a matrix structure across internal and external stakeholders.
Supports high-performing, collaborative clinical study teams.

⚖️ Equal Opportunity & Safety

BMS provides accommodations for people with disabilities.
Applicants with arrest or conviction records considered per applicable laws.
Employees encouraged to maintain COVID-19 vaccination and boosters.
Recruitment data handled per privacy regulations.

💼 Benefits & Perks

Medical, pharmacy, dental, vision care
Wellbeing programs (Living Life Better, EAP)
401(k) and financial well-being resources
Paid holidays, global shutdown, vacation (up to 120 hours), volunteer days
Parental, caregiver, bereavement, and military leave
Family care services: adoption, fertility support, traveling mothers support
Tuition reimbursement and recognition programs

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Clinical Trial Physician, Neuroscience

Job Description

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