Clinical Trial Physician

Location: Parsippany

** We Are Teva*
* We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

** Our Team, Your Impact*
* 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, working closely with Disease Area Head, Clinical Development Lead, Clinical Scientist. and other functional areas such as GCO, biostats, regulatory, pharmacovigilance.  The Director will be a key contributor to INDs, NDAs, BLAs, and other global regulatory filings and publications.

The Director will foster relationships within CDT and with opinion leaders in assigned Therapeutic area. CTP is a member of the study team and CDT.

CTP is expected to advance scientific and clinical knowledge, incorporate new methodologies, and pro-actively progress study execution.

This role is 2-3 days hybrid in our Parsippany, NJ or West Chester, PA sites.

** How You'll Spend Your Day*
* The role of CTP

+ 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

+ Manages Phase 1 - Phase 3 studies (depending on assignment) with demonstrated decision-making capabilities

+ Provides medical and scientific expertise to cross-functional colleagues

+ Designs, conducts, and reports clinical trials in line with the 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

+ May lead the CDT

+ 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 to approval phase, 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

+ Serves as the primary medical contact for assigned clinical trials, ensuring protocol adherence and safety oversight

+ Addresses medical inquiries from investigators, regulatory agencies, and internal teams, ensuring consistent application of protocol guidelines

+ Responsibility for assessment of key safety-related serious AEs in partnership with PVG and oversee narrative

+ Monitors clinical trial conduct, assessing study population, protocol adherence, data trends, safety data, adverse events (AEs), serious adverse events (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

+ Leads medical data review of trial data, including eligibility criteria

+ Supports Global Clinical Operations in clinical trial initiation, resource planning, study implementation and successful completion of study, including database lock and interim cuts. Supports site selection, patient recruitment, and investigator engagement through regular interactions and guidance

+ Leads the analysis of the benefit/risk for protocols in a matrix team environment

+ May prepare presentations and presents at relevant internal or external venues such as Investigator Meetings, independent data monitoring committees, protocol review committees, etc.

+ May participate in Site Initiation Visit (SIV) and conduct medical monitoring visits at any time during the conduct of the study to provide medical input and protocol oversight

+ Maintains strong medical and scientific reputation with the disease area and has in depth TA expertise

+ Ensure clinical trials comply with clinical guidance, ICH, GCP, in agreement with the laws of the relevant countries and Teva Standard Operating Procedures

+ Partners cross-functionally with departments such as Regulatory Affairs, CMC, Biostatistics, GCO, in the execution of Clinical Development Plans

+ Represent Teva at Scientific meetings, advisory boards, KOL interactions and meetings with regulatory agencies, as needed

+ Author and/or review abstracts, posters and manuscripts, and present data at scientific meetings, as needed

+ Maintain or establish interaction with external scientific and clinical communities and incorporate pertinent advice and learnings into the internal program.

** Travel Requirements**  **:
** Approximately…