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Strategic Alliance Lead

Strategic Alliance Lead

EORTC - European Organisation for Research and Treatment of CancerBrussels, Brussels Region, Belgium
Il y a 3 jours
Description de poste

The EORTC is seeking a dynamic Medical Doctor with a passion for oncology and a proven track record in clinical trial development to fill in the new role of Strategic Alliance Lead. Candidates interested in contributing to cutting-edge cancer research and making a real difference in patients’ lives are encouraged to apply.

The Strategic Alliance Lead will play a pivotal role in fostering and maintaining strategic partnerships with pharmaceutical, biotechnology, medical device companies and other emerging technologies. Reporting to the Headquarters Director, (s)he will work closely with internal teams and external stakeholders to bring impactful clinical trials to life.

Key Responsibilities

  • Build and maintain strategic alliances with leading pharmaceuticals, biotechnology, and life sciences companies, ensuring productive collaboration with EORTC HQ study teams and investigators.
  • Lead the trial development process from initial industry contact to clinical trial endorsement, in close collaboration with the EORTC HQ study startup team and the HQ director.
  • Contribute to developing and communicating the EORTC priorities for industry partnerships, interacting with the EORTC governance and network
  • Help plan and organize presentations of industry pipelines to relevant EORTC HQ study teams and investigators, enhancing collaboration potential.
  • Identify areas for improvement in EORTC’s interaction with industry and escalate issues when necessary.
  • Follow up on the clinical trial portfolio with industry and ensure effective progress in collaboration.
  • Intervene in case of deviations to the plan, lead collaborators to diagnose issues, and implement corrective actions.

Profile

  • Oncologist, ideally Medical Oncologist trained at a high-profile academic institution
  • Minimum 3 years of industry experience, in early or late-stage drug development
  • Thorough knowledge of Good Clinical Practice, regulatory guidelines (FDA / EMA / ICH), and clinical development processes
  • Track record of having written clinical trial protocols
  • Track record of operational excellence
  • Excellent communicator in a complex matrix environment
  • Able to travel 2-3 days a month
  • Fluent in English (written and oral)
  • Benefits

  • Permanent contract
  • Competitive salary package
  • Hybrid working environment (from Belgium only)
  • 30 days holidays (full time)
  • Meal vouchers
  • Pension plan
  • Hospitalisation insurance and ambulatory care
  • Homeworking allowance
  • Reimbursement of public transport
  • Free parking