​Consultant Clinical Program Director Opportunity - Global Oncology Program - UK

Location United Kingdom
Discipline: Clinical Operations, Clinical Research
Job type: Contract
Salary: ££ DOE
Contact name: Harry Henson

Contact email: harry.henson@rbwconsulting.com
Contact phone: 01293 364 092
Job ref: 2503HHGPD
Published: 5 days ago
Duration: 12 month contract
Expiry date: 25 Apr 2025 10:59
Startdate: ASAP

Consultant Clinical Program Director Opportunity for Global Oncology Program

Location: UK-based (Global Role)
Sector: Oncology

Are you a seasoned professional with a passion for oncology research and a track record of successful clinical program management? RBW are recruiting for a leading pharmaceutical company with a global presence, seeking a Freelance Clinical Program Director to be on of their leads for their global oncology program.

We are currently awaiting the final sign off from the client on this but are keen to have profiles to present once the role is live.

Role Overview:

As a Freelance Clinical Program Director, you will oversee the strategic planning, execution, and management of the global oncology clinical program. Your role will be pivotal in driving the success of the oncology program, ensuring alignment with regulatory standards and corporate objectives.

Key Responsibilities:

  • Clinical Program Management:

    Lead and manage global oncology clinical trials, ensuring timely and efficient execution.

  • Strategic Planning:

    Develop and implement strategic plans for the oncology program, aligning with corporate goals and regulatory requirements.

  • Regulatory Compliance:

    Ensure all clinical activities comply with international regulatory standards and guidelines.

  • Team Leadership:

    Provide leadership and direction to cross-functional teams, fostering collaboration and innovation.

  • Stakeholder Engagement:

    Engage with key stakeholders, including investigators, regulatory authorities, and internal teams, to ensure program success.

Qualifications:

  • 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.

What We Offer:

  • Opportunity to work with a leading global pharmaceutical company.

  • Competitive compensation package.

  • Flexibility to work on a contract basis, allowing for a balanced work-life schedule.

  • A chance to contribute to ground-breaking oncology research and improve patient outcomes worldwide.

If you are ready to take on a challenging and rewarding role as a freelancer, we would love to hear from you. Join our client in their mission to advance oncology research and make a global impact.