Clinical Studies Director

6 days ago

Welwyn Garden City, Hertfordshire, United Kingdom Roche Full time
About the Role

Roche is committed to fostering diversity, equity, and inclusion in our organization, reflecting the communities we serve. In our Pharmaceutical Research and Early Development organization (pRED), we strive to transform science into medicines that address unmet healthcare needs. Our mission is to make a meaningful impact on patients' lives.

Key Responsibilities
  • Lead and/or support cross-functional teams in designing and executing clinical development plans from Phase 1 through Phase 2 (proof-of-concept)
  • Coach Clinical Scientists in a line- or functional-manager status
  • Closely interface with project team leaders, safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research, and biomarker groups, and other project team members
  • Lead and/or support internal stakeholder management and governance interactions around project plans and therapeutic area strategy
  • Lead and/or support external engagements with advisory boards, site investigators, health authorities, and other key stakeholders
  • Provide clinical input to programs in discovery research
  • Lead scientific communications and disseminate the results of clinical trials in the form of conference presentations and journal publications
Requirements
  • MD or MD/PhD with a specialty in neuroimmunology, multiple sclerosis, or a similar field. Board certification and fellowship training or research experience in relevant areas is preferred.
  • At least 5 years of experience in longitudinal clinical research, preferably in drug development or clinical trials.
  • A strong track record of scientific excellence in the field, evidenced by substantial achievement in designing and implementing clinical trials and/or a high level of scholarship in industry or academia.

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