Clinical Trial Physician

vor 14 Stunden


Schweiz Modis Vollzeit

**Main responsibilities**:
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.
- Serves as a primary source of medical accountability and oversight for multiple clinical trials
- Matrix management responsibilities across the internal and external network
- Manages Phase 1 - Phase 3 studies, with demonstrated decision making capabilities
- Provides medical and scientific expertise to cross-functional colleagues

**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
- 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 safety-related 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 safety-related clinical considerations)
- Fulfills GCP and compliance obligations for clinical conduct and maintains all required training

Clinical Development Expertise & Strategy
- In collaboration with the Clinical Development Lead, 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 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, non-significant 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
- Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Keeps up-to-date 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 protocol-specific 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
**Profile**:

- MD required (or x-US equivalent)
- 5 or more years of Industry experience and/or clinical trials experience is required
- Key Competency Requirements
- Ability to communicate information clearly and lead presentations in scientific and clinical settings
- Subspecialty training in applicable therapeutic area desired: oncology, hematology, immunology and cardiovascular disease
- Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation
- Expertise in drug development process
- Expertise in the components needed to execute an effective clinical plan and protocols
- Strong leadership skills with proven ability to lead and work effectively in a team environment
- Domestic and International travel may be required.



  • Schweiz Warman O’Brien Vollzeit

    **Clinical Lead for Drug Delivery Systems** **Location: Switzerland, Belgium, or United Kingdom** **Start Date: ASAP** **Market Leading Rate** A leading global biopharmaceutical company is seeking an ambitious and passionate individual to support their clinical trials by defining and executing the strategy for drug delivery system selection. In this...


  • Schweiz NonStop Consulting Vollzeit

    We are currently hiring for a Regulatory Affairs CTA Coordinator, temporary assignment, to join a top biopharmaceutical enterprise with a diverse clinical portfolio of vaccines and therapeutics across six modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that...


  • Schweiz Johnson & Johnson Vollzeit

    For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the...


  • Schweiz Meditrial Europe Ltd. Vollzeit

    Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs, and market access. Our offices are located in Germany, Italy, Switzerland, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers unparalleled...


  • Schweiz SOPHiA GENETICS Vollzeit

    Join SOPHiA GENETICS as our new **BioPharma Business Development Director **and be responsible for building our BioPharma data partnerships throughout EMEA. This is a **remote position based in Europe**, but France, Switzerland or the UK is highly preferred. **SOPHiA GENETICS BioPharma** - Revolutionizing clinical development and commercialization of new...


  • Schweiz Alira Health Vollzeit

    **Job description**:**Position Description**: As Associate Director of Biostatistics, you will hold a combined technical and leadership position within our global Biostatistics department. You will lead Biostatistics department and projects, provide support in managing and deploying resources effectively, and work alongside the Director of Biostatistics to...

  • Cra I/cra Ii

    vor 15 Stunden


    Schweiz Labcorp Vollzeit

    Assures the implementation of project plans as assigned - Site administration and site monitoring responsibility for clinical studies according to Labcorp Drug Development Standard Operating Procedures, ICH Guidelines and GCP - Site management responsibility for clinical studies according to Labcorp Drug Development Standard Operating Procedures, ICH...


  • Schweiz NonStop Consulting Vollzeit

    On behalf of a biopharmaceutical company whose mission is to identify, develop and deliver life-changing therapies to people living with rare disease, I am currently looking for an Associate Director for the European Regulatory Affairs. The company is growing and advancing a pipeline of potential first-in-class medicines targeting rare diseases with...


  • Schweiz Johnson & Johnson Family of Companies Vollzeit

    **_ROLE DESCRIPTION_** - The Therapy Area Market Access Leader (TAMAL) for the EMEA region, reporting to the VP HEMAR EMEA, leads a team of Compound Market Access Leaders, HEMAR Managers and Strategic Pricing Managers who are accountable for delivering and executing an EMEA Market Access strategy for a portfolio of products across different stages of...