Clinical Project Physician

Vor 2 Tagen

Zug, Schweiz TN Switzerland Vollzeit
Clinical Project Physician (Rheumatology/Autoimmune) – Based Anywhere in Europe (m/w/d)

Client: Viatris

Location: Zug

Job Category: Other

Job Reference: 1c8881bda3a6

Job Views: 15

Posted: 21.01.2025

Expiry Date: 07.03.2025

Job Description:

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach, and better access to treatment.

The Role & What You Will Be Doing

Every day, we rise to the challenge to make a difference and here’s how the Clinical Project Physician role will make an impact:

  1. Join our innovative team: Together shape the future with groundbreaking Phase 3 assets, drive blockbuster growth and drive your mission and purpose to bring products to patients.
  2. Overall, the Clinical Project Physician (CPP) is responsible for providing medical leadership, oversight and guidance on clinical development projects under his/her responsibility from concept generation to design, implementation, execution, and submission/approval.
  3. Provide medical leadership internally for all TA-responsible project activities (e.g. to LCT, Clinical Team, Regulatory & Safety aspects).
  4. Provide medical and scientific input, as appropriate, to the strategic decisions of the Life Cycle Team for the assigned project(s).
  5. Contribute to global strategic development and provide evidence-based input to the clinical project related, strategic and regulatory documents.
  6. Deliver the medical components of the Clinical Development Plan (CDP) related to the project indication(s) and oversee its implementation.
  7. Contribute as needed to trial level medical activities.
  8. Ensure project(s) is/are adequately supported medically and prioritized to ensure timely and on-target delivery on set objectives and deliverables in line with clinical development goals.
  9. Provide medical input to the project-related communication/publication plan.
  10. Upon request of management, support the assessment of new in-licensing opportunities.
  11. Provide medical leadership externally based on thorough scientific review of relevant product data and consultation with internal and external experts.
  12. Lead the development and maintenance of medical interactions with key external experts and Investigators.
  13. Lead medical aspects of clinical advisory boards and study specific committees (e.g., steering committees (SC), Independent Data Monitoring Committees (IDMC), safety event committees).
  14. Contribute to clinical/scientific content for submissions to regulatory agencies and IRBs/ethics boards, answer to medical/scientific questions from Health Authorities.
  15. Be the company clinical expert at key regulatory interfaces, investigator meetings, patient organization meetings as well as partner meetings where applicable.
  16. Provide input to and execute publication and clinical communication strategy.

About Your Skills & Experience

  1. Qualified MD.
  2. Extensive experience in clinical research in a clinical research organization (CRO) or Pharmaceutical Company.
  3. Demonstrated experience in overseeing clinical projects from a medical perspective.
  4. Clinical research experience in the indication relevant to the Clinical Project is preferred.
  5. Sound knowledge of drug development based on previous deliverables.
  6. Sound knowledge of regulatory requirements/ICH guidelines.
  7. Good organizational skills, able to work as part of a cross-functional team and independently.
  8. Ability to work collaboratively in a matrix environment.
  9. Strategic thinking.
  10. Hands-on approach.
  11. Excellent written and spoken communication skills.
  12. Fluent in English (written and oral).

Benefits at Viatris

  1. Excellent career progression opportunities.
  2. Work-life balance initiatives.
  3. Bonus scheme.
  4. Health insurance.
  5. Pension.

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Viatris is an Equal Opportunity Employer.

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