Summary: The Consultant Clinical Program Director will lead the strategic planning and execution of a global oncology clinical program for a prominent pharmaceutical company. This freelance role requires extensive experience in oncology research and clinical program management, ensuring compliance with regulatory standards. The position emphasizes leadership, stakeholder engagement, and the ability to manage cross-functional teams effectively. The role offers a chance to contribute significantly to oncology research and improve patient outcomes globally.

Key Responsibilities:

• Lead and manage global oncology clinical trials, ensuring timely and efficient execution.
• Develop and implement strategic plans for the oncology program, aligning with corporate goals and regulatory requirements.
• Ensure all clinical activities comply with international regulatory standards and guidelines.
• Provide leadership and direction to cross-functional teams, fostering collaboration and innovation.
• Engage with key stakeholders, including investigators, regulatory authorities, and internal teams, to ensure program success.

Key Skills:

• Extensive experience in clinical program management within the oncology sector.
• Strong understanding of global regulatory requirements and clinical trial processes.
• Proven leadership skills with the ability to manage and motivate cross-functional teams.
• Excellent communication, organizational, and strategic planning skills.
• Ability to work independently and manage multiple priorities in a fast-paced environment.

Salary (Rate): undetermined

City: undetermined

Country: United Kingdom

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other