Clinical Program Lead – Hematology

Job Type: permanent
Region: Europe
Location: Unspecified
Posted: 1st November 2019

I am currently working with a leading global clinical trials company seeking two experienced physicians within Phase I – Phase III clinical development. One role will focus on early phase and the other role focused in late stage clinical development of innovative molecules for the treatment of multiple disease areas within Oncology, Haematology or Paediatrics.

The Role(s):

The role is responsible for input and oversight for early / late stage clinical development plans within the Oncology, Haematology or Paediatrics department, from pre-clinical research, First in Man studies through Phase I / II / III Clinical Trials.

The successful applicant(s) will be responsible for leading the development of key products in these areas. The main purpose of the role will be to oversee a series of Oncology, Haematology or Paediatrics trials, draft study specific documentation such as NDA / CTA submissions and Investigator Brochures, alongside reviewing study data and providing expert advice to aid in the development of their Oncology, Haematology or Paediatrics portfolio.

Further Key Responsibilities:

  • Directing and overseeing clinical research plans, and providing input to help integrate the Clinical Development Plan with the Drug Development Plan
  • Serving as the clinical / medical team expert to provide direction to all project team functions, regularly liaising with KOL’s and organizing Advisory Board Meetings
  • Implementing strategies to identify, monitor and resolve clinical / program trial issues
  • Reviewing / monitoring safety study data and providing clinical expertise and content to regulatory documents
  • Proactively and independently find solutions and drive innovation

Your Background:

  • Educated to Medical Degree
  • Board Certification / specialist training required (Oncologist, Hematologist or internal medicine)
  • Demonstrable experience in Phase I-III clinical trial management
  • Investigator experience
  • Ability to influence others; self-starter with an inquisitive nature and practical approach to problem solving
  • Demonstrated competence as Study Director / Medical Monitor / Research Physician / Medical Advisor and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required but is preferred

If you’re interested, get in touch with me ASAP…

Adam Bloomfield

Clinical Development and Medical Affairs Consultant

Email: abloomfield (at) barringtonjames.com

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