Medical Director Clinical Development – Radiopharm

Job title:

Medical Director Clinical Development – Radiopharm

Company

Skills Alliance

Job description

Job Description(Associate) Medical Director Clinical Development – RadiopharmaceuticalsLocation: Remote – UKOur client is a clinical-stage radiopharmaceutical company committed to developing novel targeted radiopharmaceutical treatments for cancer. With established leadership and extensive experience in therapeutic radiopharmaceuticals, our client boasts a robust pipeline of precisely targeted radiopharmaceuticals. Initially, their efforts are concentrated on prostate cancer, with intentions to broaden their focus to other cancer types in the future.The position will provide key overall clinical, scientific and/or logistical support to clinical development programs as well as working closely with the cross-functional teams, the seniority and level of responsibilities will be adjusted to the successful applicant.This is an excellent opportunity for a first-to-industry physician with a speciality in Radio-oncology or a pharmaceutical physician looking to step into Radiopharmaceuticals.Primary Responsibilities:

• Conduct and have oversight over medical monitoring activities.
• Ensure the efficient planning, implementation, and interpretation of clinical studies, including medical monitoring, synopsis/protocol development data analysis and writing of final reports.
• As the primary medical monitor for assigned study(ies), be the first point of contact with sites; answer site questions about eligibility, enrolment; safety and patient management, working in close contact with the CRO.
• Build and implement global clinical development plans consistent with the Company’s strategic vision and mission.
• Interact frequently with sites to support study awareness, patient recruitment, and quality of study conduct.
• Communicate appropriate program issues and results to key internal and external partners.
• Support regulatory interactions, including the submission of regulatory documents and presentations.
• Provide clear and insightful clinical and scientific expertise to advance the successful transition of compounds from discovery to full development, and subsequently to life cycle management.
• To Support the review of business development & learning activities
• Align with current local and international regulations, laws, scientific and regulatory guidance, and Good Clinical Practices.
• Other duties as assigned.

Requirements:

• MD required. Board Certified/Board Eligible in Oncology/Radio-oncology.
• GMC Registered
• Previous Clinical Research experience, as a sub/principal investigator or study physician.
• Thorough working knowledge/understanding of clinical trial design, methodology and statistical concepts.
• Proven ability to interact with different functional groups, investigators, key opinion leaders and the medical/scientific community.
• Ability to thrive in a fast-paced, dynamic small company environment with the ability to adjust workload based upon changing priorities.
• Ability to engage in an open, constructive, and continuous dialogue with the Company’s partners based on equality and mutual respect; transparency is an essential element to success.
• Willingness to travel nationally and internationally, this will be approx. 25%.

Our client is an equal-opportunity employer and is committed to diversity and inclusion inthe workplace. We encourage applications from candidates of all backgrounds andexperiences.

Expected salary

Location

United Kingdom

Job date

Sat, 29 Jun 2024 22:07:21 GMT

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