Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options?

My client manages the entire life cycle of the drug development process; we are looking to expand within Oncology and Haematology Drug Development. With >250 clinical trials completed within the last 5 years, my client is a world leader in developing clinical trials and bringing new therapeutics to the market.

If you have a clinical background in Internal Medicine, Oncology or Haematology and experience leading clinical trials as a medical monitor, investigator or study physician, please see below.

Key responsibilities

  • Provide medical expertise across the entire scope of clinical development and medical affairs
  • Develop and deliver expert training programs
  • Represent Medical Affairs within Legal, Medical and Regulatory review committees
  • Apply medical and clinical expertise to inspire internal teams and external customers
  • Build and develop business relationships with Key Opinion Leaders
  • Collaborate with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan
  • Provide oversight of strategic clinical trial progression across a variety of indications and therapy areas related to solid tumours or malignant haematology.

Requirements

  • Medical Doctor (M.D, MBBS, MBChB or equivalent)
  • PhD advantageous
  • >3 years clinical trials experience within Oncology or Haematology
  • Investigator experience on clinical trials phase II-III
  • Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal
  • Demonstrated competence as a Research Physician / Study Director / Medical Monitor / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician
  • Prior experience working with the FDA or EMA on responses to inquiries for study related information

Benefits

  • Highly competitive basic salary
  • Private Healthcare
  • Excellent bonus scheme
  • Clear internal promotion pathway
  • Remote working flexibility
  • Opportunity to travel the world
  • Strategic oversight on multiple clinical programs

Get in touch…

About Your Consultant

I am a Senior Specialist Clinical Development, and Medical Affairs Consultant covering the European region. The pharmaceutical industry is a genuine passion of mine having attained first-class classification in both my Biomedicine BSc. and a Molecular Medicine MSc. Therefore, I maintain expert-level, credible, knowledge within the European market with insights on the lastest development programs. Thus, I strongly believe in the importance of finding the most-suitable candidates for any of my clients. My predominant focus at BarringtonJames is to apply my extensive knowledge, experience, and resources in sourcing only the most specific and best candidates for life science companies.

Email: abloomfield@barringtonjames.com Telephone: 01293776644

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