Clinical Study Physician - Dermatology & GI

Overview

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. We’re dedicated to addressing patients’ needs now and in the future, with a high-performing, inclusive culture that values fresh thinking and collaboration. You’ll have room to grow, flexibility to balance life with work, and the opportunity to better health worldwide, together.

The Clinical Trial Physician (CTP), Director, sits within Clinical Development and is responsible for contributing to the design and implementation of the clinical development plan. This role works closely with the Disease Area Head, Clinical Development Lead, Clinical Scientist, and other functional areas such as GCO, biostatistics, regulatory, and pharmacovigilance. The Director will contribute to INDs, NDAs, BLAs, and other global regulatory filings and publications, and will foster relationships with opinion leaders in the assigned therapeutic area.

The CTP is a member of the study team and CDT. The CTP is expected to advance scientific and clinical knowledge, incorporate new methodologies, and proactively progress study execution.

• Serve as a primary source of medical accountability and oversight for one or more clinical trials
• Matrix management responsibilities across the internal and external network
• Manage Phase 1 – Phase 3 studies (depending on assignment) with demonstrated decision-making capabilities
• Provide medical and scientific expertise to cross-functional colleagues

Travel Requirements: Approximately 20%, both domestic and international.

Location: The selected candidate will ideally work a hybrid schedule (2–3 days/week onsite) in either Parsippany, NJ or West Chester, PA. We may consider remote flexible arrangements where necessary due to location. If remote, occasional travel to one of our offices will be required as needed.

• Designs, conducts, and reports clinical trials in line with development, regulatory and global program strategy. Provides medical expertise in study design, protocol development, and execution, collaborating with cross-functional teams to advance clinical programs.
• Contributes to and supports the development and execution of the CDP in collaboration with the CDL or DAH, including clinical development strategy from early development through approval, sections of the IDP and TPP.
• Accountable for protocol concept sheet, final protocol and protocol amendments.
• Ensure continuous medical review of aggregated data during clinical trial conduct to identify trends and ensure quality data for database locks and interim cuts.
• Serve as the primary medical contact for assigned clinical trials, ensuring protocol adherence and safety oversight.
• Address medical inquiries from investigators, regulatory agencies, and internal teams, ensuring consistent application of protocol guidelines.
• Responsible for assessment of key safety-related serious AEs in partnership with PVG and oversee narrative.
• Monitor clinical trial conduct, assessing study population, protocol adherence, data trends, safety data, AEs, SAEs, and emerging safety signals.
• Review documents supporting clinical development such as Investigator’s brochure, regulatory documents for IND/CTA, clinical sections of integrated development plans, and submission dossiers for regulatory approval.
• Lead medical data review of trial data, including eligibility criteria.
• Support Global Clinical Operations in trial initiation, resource planning, study implementation and successful completion, including database lock and interim cuts. Support site selection, patient recruitment, and investigator engagement through regular guidance.
• Lead the analysis of benefit/risk for protocols in a matrix team environment.
• Present at Investigator Meetings and other relevant venues such as data monitoring and protocol review committees.
• May participate in Site Initiation Visit (SIV) and conduct medical monitoring visits to provide input and protocol oversight.
• Maintain strong medical and scientific reputation with the disease area and have in-depth TA expertise.
• Ensure trials comply with clinical guidance, ICH, GCP, and…