Clinical Trial Physician - Boudry, Schweiz - Bristol Myers Squibb

Bristol Myers Squibb
Bristol Myers Squibb
Geprüftes Unternehmen
Boudry, Schweiz

vor 1 Woche

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter
Beschreibung

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity.

Take your career farther than you thought possible.

Position Summary


The Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development.

Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials.

  • Manages data review and quality of Phase
  • Phase 3 studies, with demonstrated analytical and decisionmaking capabilities
  • Serves as a primary source of medical accountability and oversight for clinical trials
  • Matrix management responsibilities across the internal and external network
  • Provides medical and scientific expertise to crossfunctional BMS colleagues
Key Responsibilities

Clinical Data Review and Oversight for Immunologic/ Rheumatologic Indications

  • Leads eligibility and clinical efficacy data review and monitoring activities across one or more studies/indications
  • Delivery and development of indication
- and study-specific trainings

  • Manages site interactions for medical questions and education related to protocolspecific eligibility and ongoing efficacy assessments
  • Fulfills GCP and compliance obligations for clinical conduct and maintains all required training
Medical Monitoring

  • Contributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT)
  • Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)
  • Holds responsibility for assessment of key safetyrelated serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
  • Collaborates with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safetyrelated clinical considerations)
Clinical Development Expertise & Strategy

  • In collaboration with the Clinical Development Lead, may design and develop clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets
  • Provides oversight and medical accountability for a group of studies
  • Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists
  • Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, nonsignificant deviations etc.)
  • Identifies and builds relationships with principal investigators and site personnel. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs
  • Maintains a strong medical/scientific reputation within the disease area. Has knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Keeps uptodate in the disease area by attending scientific conferences and ongoing review of the literature
  • Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape
  • Provides ongoing medical education in partnership with CS to allow for protocolspecific training, supporting the study team, investigators, and others
Health Authority Interactions & Publications

  • Contributes to key Health Authority interactions and advisory board meetings as Clinical Trial Physician
  • Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with Clinical Scientists
Qualifications & Experience

  • MD/DO required (or exUS equivalent)
  • 3 or more years of clinical experience and/or clinical trials experience (within industry/CRO or academia as investigator) required
  • Experience in clinical data review, analysis and interpretation/integration required
  • Ability to communicate and present information clearly in scientific and clinical settings
  • Subspecialty training or experience in immunology therapeutic area, especially SLE is highly desired
  • Knowledge of global drug development and t