Global Clinical Trials Specialist
This role oversees the development of clinical trials, including medical oversight and strategic planning for portfolio and protocol feasibility.
The Global Clinical Trials Specialist will ensure compliance with all aspects of clinical trials and related activities, maintaining effective communication and stakeholder management both locally and globally.
Key Responsibilities:
* Provide medical oversight and contribute to operational trial deliverables across all stages.
* Drive portfolio/trial medical feasibility and provide country clinical strategic guidance and proposals.
* Analyse and identify new sites for clinical trials, assessing capability, patient pool, and country treatment landscape, and make recommendations for potential inclusion.
* Develop and provide robust indication and protocol training to CRAs, CSMs, RSMs, and other functions in the country.
* Ensure medical education, implementation, and compliance to protocols, standards (SOPs), and best practices for clinical development.
* Collaborate cross-functionally for early product launch planning processes.
Essential Requirements:
* Medical Degree (MD, MBBS).
* Proven experience in medical practice or pharmaceutical industry experience with a background in clinical trials/medical affairs/life sciences/research.
* Experience in Haematology and Oncology clinical trials is valuable.
* Demonstrated experience in managing projects, feasibility conduct, and executing strategic plans from a medical perspective.