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Director- Clinical Development

Director- Clinical Development

Posted 12 March by IMC LOCUMS LIMITED
Easy Apply Featured Ended
USD$240,000 - USD$280,000 per annum
Milton Park Industrial Estate , Oxfordshire
Permanent, full-time
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Posted by IMC LOCUMS LIMITED


About the Company:
Our client (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company dedicated to developing and commercializing transformative medicines for oncology, infectious diseases, and autoimmune diseases. Our R&D leaders are internationally recognized as industry trailblazers. We foster an environment of innovation, collaboration, and diversity, seeking talented individuals to join us in delivering new medicines to patients.

Key Responsibilities:

  • Lead clinical development strategy and plans, collaborating with Development and Discovery Program Leads and other cross-functional teams.
  • Design high-quality clinical trial protocols aligned with product strategy and development plans.
  • Establish strong relationships with key opinion leaders and partners to support external collaborations.
  • Provide medical oversight of clinical studies, including medical monitoring, data review, interpretation, and reporting.
  • Contribute to regulatory strategy, submissions, and global health agency meetings.
  • Assist in business development activities as requested.
EXPERIENCE & KNOWLEDGE:

  • Demonstrated ability to build relationships and troubleshoot challenges within teams.
  • MD or MD/PhD with a clinical perspective and exceptional achievement in oncology therapy development.
  • Strategic thinker with success in designing innovative clinical trials.
  • Strong communication skills and ability to engage stakeholders at all levels.
  • Collaborative and able to motivate cross-functional team members.
  • Thorough understanding of drug development process and regulatory requirements.

EDUCATION & QUALIFICATIONS:

  • MD or MD/PhD with research training.
  • Working knowledge of basic and clinical science.
  • Strong understanding of pharmacokinetics, biomarkers, statistical principles, and regulatory requirements.
  • At least 3 years of relevant experience in clinical drug development, including early phase trials.
  • At least 2 years of experience as a medical monitor in biotechnology/pharmaceutical industry or CRO.

Benefits:

This position is eligible for standard company benefits, including medical, dental, vision, time off, and 401k, as well as participating in our client's annual incentive plans. Actual compensation may vary based on geographic location, work experience, education, and skill level.

Annual Salary Range (US Remote):
$240,000 - $280,000

Reference: 52295296

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