Medical Director, Clinical Development (Oncology) – 12‑Month Freelance Contract
Overview
One of the world’s leading global pharmaceutical companies is seeking an experienced Medical Director, Clinical Development to support its expanding oncology portfolio. This 12‑month freelance contract offers the opportunity to play a key leadership role in the design, execution, and strategic oversight of Phase I–IV oncology clinical trials across a diverse and innovative pipeline.
The ideal candidate is a board‑certified Oncologist, Hematologist, or Immunologist with deep expertise in global clinical development, protocol design, and cross‑functional leadership in complex oncology programs.
Key Responsibilities
Clinical Development Leadership
* Provide medical leadership for oncology programs spanning early‑phase to late‑phase (I–IV) clinical trials.
* Lead the development, review, and approval of clinical protocols, amendments, IBs, CSRs, and other core clinical documents.
* Ensure scientific and medical excellence across all study activities, from concept through execution and reporting.
Safety & Medical Oversight
* Serve as the medical expert for assigned studies, including ongoing safety monitoring, data review, and clinical decision‑making.
* Collaborate with pharmacovigilance teams to evaluate safety signals and contribute to risk–benefit assessments.
Cross‑Functional Collaboration
* Partner closely with clinical operations, biostatistics, regulatory affairs, translational medicine, and commercial teams to ensure alignment and successful trial delivery.
* Provide medical input into regulatory submissions, responses, and interactions with global health authorities.
Strategic Contribution
* Contribute to the long‑term clinical development strategy for key oncology assets.
* Support portfolio prioritization, indication selection, and evidence‑generation planning.
Required Qualifications
* Medical degree (MD or equivalent) with specialization in Oncology, Hematology, or Immunology.
* Significant experience in global clinical development within the pharmaceutical or biotech industry.
* Proven track record in protocol design, clinical trial execution, and medical oversight across Phase I–IV oncology trials.
* Strong understanding of tumor biology, immuno‑oncology, and emerging therapeutic modalities.
* Experience interacting with global regulatory agencies (FDA, EMA, PMDA, etc.).
* Excellent communication skills and the ability to operate effectively in a highly matrixed, multinational environment.
Contract Details
* Duration: 12 months (freelance/independent contractor)
* Engagement: Full‑time, remote or hybrid depending on location and project needs
* Client: One of the top global pharmaceutical companies with a world‑class oncology pipeline
Ideal Candidate Profile
You thrive in fast‑moving, scientifically rich environments and bring a blend of clinical expertise, strategic thinking, and operational excellence. You’re comfortable leading complex global studies, influencing cross‑functional teams, and shaping the future of oncology drug development.