P2429 - Associate Medical Director Oncology

vor 19 Stunden

Lausanne, Schweiz Debiopharm Vollzeit

Debiopharm is a privately-owned Swiss biopharmaceutical company committed to research in oncology and infectious diseases to improve patient outcomes and quality of life. Debiopharm International SA aims to develop innovative therapies via our unique “development only” business model, acting as a bridge between disruptive discovery products and patient access in international markets. At Debiopharm, you will be at the forefront of the fight against cancer and infectious diseases through working on innovative medicines for patients. Join our team at Debiopharm where together, we innovate, we impact, and we grow.

For our Clinical Development organization based at our Headquarters in Lausanne, we are looking for

Associate Medical Director Oncology

As an Associate Medical Director in Clinical Development, you will play a pivotal role in shaping the future of patient care. Working closely with our dynamic team, you will oversee the planning, execution, and interpretation of Phase I to III clinical studies in oncology, driving forward our clinical development programs with passion and expertise.

Your responsibilities will be but not limited to:

  1. Develop clinical strategy for the therapeutic area in the assigned programs, taking into account medical practice and unmet medical need.
  2. Provide clinical leadership and medical strategic input for all clinical deliverables in the assigned program(s).
  3. Collaborate closely with cross-functional teams to execute clinical studies and support the overall Clinical Development Plan.
  4. Design and implement study protocols, ensuring adherence to the highest standards of scientific rigor and ethical conduct.
  5. Foster strategic partnerships with key stakeholders including Pharmacovigilance, Clinical Operations, Regulatory Affairs, and Biostatistics to ensure seamless study execution.
  6. Provide insightful analysis and interpretation of clinical data, driving evidence-based decision-making and shaping our scientific strategy.
  7. Engage with key opinion leaders to share knowledge, gather insights, and advance our understanding of oncology therapeutics.
  8. Ensure compliance with regulatory requirements and uphold the highest standards of Good Clinical Practice in all aspects of research conduct.

Your qualifications include:

  1. Medical oncologist working in Academia/hospital as Doctor, with prior experience as an investigator and/or sub-investigator on clinical trials in oncology and/or with prior experience in pharma/biotech in clinical trials/clinical development.
  2. Proven track record of staying abreast of the latest developments in clinical practice and scientific progress.
  3. Strong communication skills in English, with the ability to articulate complex medical concepts to diverse audiences.
  4. A collaborative mindset, coupled with leadership abilities and a drive for innovation in a fast-paced environment.
  5. Knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory requirements.

What we offer:

  1. International, highly dynamic environment with a long-term vision.
  2. Cross-functional collaboration at the forefront of the most advanced scientific developments in oncology and the anti-bacterial industry.
  3. Exposure to a wide variety of areas and functions within clinical development and the pharmaceutical industry.
  4. Participation in a company where innovation, people, and entrepreneurship are the fundamental keys to success.
  5. Proud to be an Equal-Pay certified, we ensure offering all our employees the same opportunities.
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