Director, Clinical Development & Trial Medicine

Teva Pharmaceuticals

Parsippany-Troy Hills (NJ)

Hybrid

USD 232,000 - 289,000

Full time

14 days+
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Job summary

Teva Pharmaceuticals is seeking a Director-level Clinical Trial Physician to contribute to the design and execution of the global clinical development plan. The role partners with Disease Area Heads and cross-functional teams to advance trials from early development through approval, while ensuring regulatory and safety standards are met.

The position offers a hybrid work arrangement at Parsippany, NJ or West Chester, PA, with opportunities to lead CDT activities, review regulatory documents,

Qualifications

  • MD or DO with immunology expertise and experience in GI, dermatology, or rheumatology.
  • Knowledge of regulatory requirements for clinical trials and IND/CTA processes.
  • Experience designing and executing Phase 1–3 clinical trials.

Responsibilities

  • Serve as primary medical accountability and oversight for one or more trials.
  • Provide medical and scientific input to cross-functional teams and study design.
  • Lead data review, safety oversight, and BD/IDP alignment with CDP strategy.
  • Manage protocol concepts and amendments; support regulatory submissions and publications.
  • May lead the CDT and engage with investigators, sites, and external partners.

Skills

Interpersonal communication
Verbal communication
Written communication
Multitasking
Time management

Education

MD, DO
Immunology experience
GI, dermatology or rheumatology knowledge

Job description

Teva Pharmaceuticals is seeking a Director-level Clinical Trial Physician to contribute to the design and execution of the global clinical development plan. The role partners with Disease Area Heads and cross-functional teams to advance trials from early development through approval, while ensuring regulatory and safety standards are met.

The position offers a hybrid work arrangement at Parsippany, NJ or West Chester, PA, with opportunities to lead CDT activities, review regulatory documents,

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