Global Clinical Program Lead - Oncology

England (GB) or Germany (DE)
Salary
Comprehensive Salary, Enhanced Bonus Scheme, Company Car, Private Health + Package
Start date
3 Jul 2020
Closing date
2 Aug 2020
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Discipline
Clinical Research
,
Clinical Development
,
Investigator
,
Medical Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Director/Executive
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Job Details
Company

Job Details

Are you a physician with a strong research background in Oncology or Haematology?
Do you feel as though you could apply your medical expertise to enhance drug development within the fields of Oncology or Haematology?
250 clinical trials completed within the last 5 years in these therapeutic areas, my client is a world leader in oncology and haematology drug development.

Key responsibilities

• Provide medical expertise at the global level across the entire scope of the drug development process
• Develop and deliver expert training programs
• Represent the clinical development team within Legal, Medical affairs and Regulatory review committees
• Apply medical and clinical expertise to inspire internal teams and external customers
• Build and develop business relationships with potential clients and Key Opinion Leaders (KOLs)
• Collaborating with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plan
• Oversee strategic clinical trial progression across a variety of tumour sub-types and therapy areas.
• Autonomy within a cross-functional collaborative team environment

Requirements

• Medical Doctor (M.D, MBBS, MBChB or equivalent)
• PhD advantageous
• Clinical specialisation in Oncology, Hematology, Paediatrics’ or Internal medicine
• Experience in Oncology or Hematology clinical trials is essential
• Investigator experience in clinical trials is preferred
• Experience in phase II-III clinical trials is advantageous
• Experienced writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal
• Demonstrated competence as a 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

Benefits

• Comprehensive salary
• Enhanced bonus scheme
• Company Car
• Market leading Pension Scheme
• Private Health Insurance
• Relocation package
• Travel allowance
• 30+ days holiday
• Clear development pathway

Get in touch...

• Contact: Adam J. Bloomfield BSc. MSc.
• Senior Clinical Development and Medical Affairs Recruitment Consultant
• Email:

abloomfield (@) barringtonjames.com

Company

We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Company info

Website
https://barringtonjames.com/
Telephone
01293 776644
Location
The Galleria
Station Road
Crawley
West Sussex
RH10 1WW
United Kingdom
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