Medical Director, Global Clinical Development, Oncology

About The Opportunity
Our client is a global science and technology company with a growing healthcare business. They develop innovative medicines for patients across several therapeutic areas, with oncology at the core of their pipeline. They offer a diverse, inclusive and flexible culture, with real scope for personal development and career progression.
The role
As Medical Director in Global Clinical Development Oncology, you will provide clinical and scientific leadership for oncology development programs. Experience in targeted therapies, antibody-drug conjugates (ADCs) and/or immuno-oncology is ideal. Solid tumor drug development experience is expected, and hematology/hematologic oncology experience is viewed favorably.
You will independently drive day-to-day clinical development activities while contributing to the overall clinical strategy in a global matrix environment.
Key Responsibilities
Lead assigned clinical studies and contribute to broader program strategy from Phase 1 through Phase III, including registration-enabling activities, regulatory submissions and Health Authority interactions
Integrate clinical, translational, biomarker and emerging data to support indication strategy, patient selection, dose strategy and key development decisions
Act as a core member of cross-functional teams and the Global Project Team, partnering with Program Leadership, Translational Medicine, Biostatistics, Clinical Pharmacology, Regulatory Affairs, Clinical Operations, Safety and Medical Writing
Support study design, dose strategy and indication prioritization
Provide medical monitoring and clinical oversight for assigned studies
Review and interpret safety and efficacy data to support study decisions
Author and contribute to key clinical and regulatory documents, including protocols, investigator brochures, clinical study reports, briefing books, submission documents and dossiers
Support interactions with Health Authorities and internal governance bodies
Drive delivery of milestones across global teams and timelines
Contribute to a high-performing, collaborative matrix environment
Minimum Qualifications
MD with expertise in clinical drug development and required expertise in oncology
3+ years of industry experience in clinical R&D within pharma or biotech
Experience supporting or leading clinical studies across Phase 1 to Phase III
Experience contributing to clinical development strategy, regulatory submissions and registration-enabling activities
Familiarity with clinical dossiers, regulatory documentation and Health Authority interactions
Demonstrated ability to integrate translational and biomarker data into development decisions
Experience working in cross-functional, matrixed, international teams
Familiarity with ICH-GCP, FDA and/or EMA expectations and clinical trial regulations
Strong written and verbal communication skills in English
Ability to work independently, manage multiple priorities and collaborate across time zones in an office-based environment
Preferred Qualifications
Experience in targeted therapies, ADCs, immuno-oncology and/or hematology/hematologic oncology
Experience across early and late clinical development
Experience contributing to study designs that support potential registration pathways
Experience in precision medicine and/or biomarker-driven development
Strong project leadership, with a track record of driving timelines and decision points
Board certification in Medical Oncology/Hematology or a relevant subspecialty