Associate Clinical Trial Physician, Oncology - Boudry, Schweiz - Bristol Myers Squibb

Bristol Myers Squibb
Bristol Myers Squibb
Geprüftes Unternehmen
Boudry, Schweiz

vor 1 Monat

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.


Functional Area Description


The Associate 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.


Position Summary / Objective

  • Supports a CTP or senior CTP
  • Matrix management responsibilities across the internal and external network
  • Supports medical monitoring of Phase
  • Phase 3 studies
  • Provides medical expertise to crossfunctional BMS colleagues

Position Responsibilities
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)
  • Conducts medical data review of trial data, including eligibility review, as directed by a CTP or senior CTP
  • Holds responsibility for site interactions as delegated by the study CTP/senior CTP in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)
  • Supports the CTP/senior CTP with assessment of key safetyrelated serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
  • Collaborates with CS and inputs into protocols (input on inclusion/exclusion and other safetyrelated clinical considerations)
  • Fulfills GCP and compliance obligations for clinical conduct and maintains all required training
Clinical Development Expertise & Strategy

  • In collaboration with the study CTP, designs and develops 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 study
  • Supports 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. 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
  • Develops and maintains a strong medical/scientific reputation within the disease area. Has indepth 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 Associate 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

Degree Requirements
MD required (or x-US equivalent)


Experience Requirements
3 or more years of clinical practice experience and/or subspecialty training is preferred


Key Competency Requirements

  • Ability to communicate and present information clearly in clinical settings
  • Interest in the scientific method to test hypotheses, including statistical design, analysis, and interpretation
  • Strong leadership skills with proven ability to lead and work effectively in a team environment
  • Ability to learn and function in diverse and complex or matrix environments

Travel Required
Domestic and International travel may be required.


Uniquely Interesting Work, Life-changing Careers

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, empl
Mehr Jobs von Bristol Myers Squibb
Alle Jobs von Bristol Myers Squibb anzeigen