Clinical Trial Physician
Teva Pharmaceuticals
August 22, 2026
Remote friendly (Parsippany, NJ)
United States
Clinical Research and Development
Clinical Trial Physician (CTP), Director
Responsibilities:
- Serve as primary medical accountability/oversight for one or more clinical trials; matrix manage internal/external networks.
- Manage Phase 1–3 studies (assignment-dependent); provide medical and scientific expertise to cross-functional teams.
- Design, conduct, and report clinical trials aligned to development/regulatory/global program strategy; lead or contribute to the Clinical Development Plan (CDP) execution from early development through approval.
- Accountable for protocol concept sheet, final protocol, and protocol amendments.
- Ensure continuous medical review of aggregated data; act as primary medical contact ensuring protocol adherence and safety oversight.
- Address medical inquiries from investigators, regulatory agencies, and internal teams; assess key safety-related serious AEs with PVG and oversee narrative.
- Monitor trial conduct (population, protocol adherence, data trends, AEs/SAEs, emerging safety signals) and lead benefit/risk analysis.
- Review key documents (e.g., Investigator’s brochure, IND/CTA regulatory documents, integrated development plan sections, submission dossiers); lead medical data review including eligibility criteria.
- Support Global Clinical Operations for initiation, resource planning, implementation, database lock/interim cuts, site selection, recruitment, and investigator engagement.
- May lead CDT; may present at investigator meetings/committees; may conduct SIV and medical monitoring visits.
Education/Requirements:
- MD or DO.
- At least 3 years in pharma/CRO/health science with experience planning/managing clinical trials or deep clinical principles/therapy knowledge.
- Knowledge of regulatory requirements; experience designing/executing clinical trials.
- May have performed protocol design academically and/or served as assistant/Principal Investigator; may have been an FDA reviewer.
Preferred:
- Immunology therapeutic area expertise; experience in GI, dermatology, and/or rheumatology.
Skills/Competencies:
- Excellent English scientific communication; manage multiple competing priorities.
- Strong urgency/time-pressure management; thrive independently.
- Professional interface with internal/external stakeholders.
Travel: ~20% (domestic and international).
Hybrid: 2–3 days in Parsippany, NJ or West Chester, PA.
Salary range: $231,520–$289,400 annually.
Benefits (selected): Comprehensive health insurance; 401(k) match up to 6% and annual 3.75% defined contribution; paid time off; company-paid life/disability; additional listed benefits.
Application instruction:
- If already working at Teva, apply via the internal career site on Twist.
Responsibilities:
- Serve as primary medical accountability/oversight for one or more clinical trials; matrix manage internal/external networks.
- Manage Phase 1–3 studies (assignment-dependent); provide medical and scientific expertise to cross-functional teams.
- Design, conduct, and report clinical trials aligned to development/regulatory/global program strategy; lead or contribute to the Clinical Development Plan (CDP) execution from early development through approval.
- Accountable for protocol concept sheet, final protocol, and protocol amendments.
- Ensure continuous medical review of aggregated data; act as primary medical contact ensuring protocol adherence and safety oversight.
- Address medical inquiries from investigators, regulatory agencies, and internal teams; assess key safety-related serious AEs with PVG and oversee narrative.
- Monitor trial conduct (population, protocol adherence, data trends, AEs/SAEs, emerging safety signals) and lead benefit/risk analysis.
- Review key documents (e.g., Investigator’s brochure, IND/CTA regulatory documents, integrated development plan sections, submission dossiers); lead medical data review including eligibility criteria.
- Support Global Clinical Operations for initiation, resource planning, implementation, database lock/interim cuts, site selection, recruitment, and investigator engagement.
- May lead CDT; may present at investigator meetings/committees; may conduct SIV and medical monitoring visits.
Education/Requirements:
- MD or DO.
- At least 3 years in pharma/CRO/health science with experience planning/managing clinical trials or deep clinical principles/therapy knowledge.
- Knowledge of regulatory requirements; experience designing/executing clinical trials.
- May have performed protocol design academically and/or served as assistant/Principal Investigator; may have been an FDA reviewer.
Preferred:
- Immunology therapeutic area expertise; experience in GI, dermatology, and/or rheumatology.
Skills/Competencies:
- Excellent English scientific communication; manage multiple competing priorities.
- Strong urgency/time-pressure management; thrive independently.
- Professional interface with internal/external stakeholders.
Travel: ~20% (domestic and international).
Hybrid: 2–3 days in Parsippany, NJ or West Chester, PA.
Salary range: $231,520–$289,400 annually.
Benefits (selected): Comprehensive health insurance; 401(k) match up to 6% and annual 3.75% defined contribution; paid time off; company-paid life/disability; additional listed benefits.
Application instruction:
- If already working at Teva, apply via the internal career site on Twist.