Live opening · Posted 10 days ago

Medical Director / Senior Medical Director – Oncology Clinical Development

Oncostrata · United Kingdom (Remote)
Linkedin No
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At a glance

The key details from the original listing.

Posted 10 days ago
CompanyOncostrata
LocationUnited Kingdom (Remote)
Work modeNo
SourceLinkedin
Listed10 days ago

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About the role

Description supplied by the original job listing.

The Opportunity
We are seeking an experienced Medical Director with expertise in lung cancer drug development to provide medical leadership across ongoing and planned clinical development programmes.
Working closely with cross-functional teams, you will support clinical strategy, protocol development, medical monitoring, data review, safety oversight, and regulatory activities. This role is suited to a physician with pharmaceutical and/or biotechnology industry experience who can combine strategic clinical development input with hands-on study support.
Key Responsibilities
Provide medical leadership across lung cancer clinical development programmes.
Contribute to clinical development strategy, study design, and protocol development.
Provide medical monitoring support for ongoing clinical trials.
Review and interpret clinical and safety data to support programme decisions.
Participate in safety review meetings and benefit-risk assessments.
Support investigator interactions and provide medical guidance during study conduct.
Contribute to regulatory submissions and health authority interactions.
Support scientific communications, publications, congress activities, and advisory boards.
Monitor developments in the thoracic oncology landscape and competitive environment.
Candidate Profile
Essential
MD, MBBS, or equivalent medical qualification.
Specialist training in Medical Oncology.
Previous experience as a Medical Director, Clinical Development Physician, or Senior Medical Monitor within the pharmaceutical or biotechnology industry.
Significant expertise in lung cancer and precision oncology.
Experience with targeted therapies, immuno-oncology agents, and/or antibody-drug conjugates (ADCs).
Strong understanding of clinical drug development, regulatory requirements, and ICH-GCP.
Experience supporting Phase I-III oncology clinical trials.
Excellent scientific communication and stakeholder management skills.
Preferred
Experience supporting global clinical development programmes.
Experience with regulatory submissions and health authority interactions.
Experience across both early- and late-stage oncology development.
About Oncostrata
Oncostrata is a specialist oncology clinical development consultancy focused exclusively on cancer drug development. We partner with pharmaceutical and biotechnology companies as embedded members of sponsor teams, providing clinical development, medical monitoring, medical leadership, and strategic scientific support across oncology programmes. Our work is dedicated solely to oncology, allowing us to provide deep therapeutic expertise and experienced clinical development leadership across the development lifecycle.

Work arrangement
No

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