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Job Details

Clinical Due Diligence Manager

Company: Barrington James Europe
Reference: BS-CDDM-1
Closing Date: 14 Mar 18
Type: Full Time
Salary (£): Negotiable

Job Summary:

My client are I are searching for a Clinical Due-Diligence Manager to join their Operations team within a leading Generics company in the German market, focusing on Global Business Development.



  • The candidate will be seen as a biopharmaceutical and clinical expert
  • 3 years minimum of clinical research experience alongside grounded clinical experience
  • Competent understanding and knowledge of pharmacokinetics, bio-analytics, toxicological and clinical studies, will preference being shown to those who have had experience within the management of phase III studies
  • 2 years minimum experience with clinical due diligence (evaluation) and the arrangement of clinical programmes in association with external business development partners
  • High levels of communicational and presentational skills, with the ability to interpret, analyse and discuss data
  • Result orientated
  • Must have shown experience working within a functional, global and cross-company teams
  • Graduated in natural sciences (pharmacy, chemistry, biology or equivalent)
  • Strong degree of computer literacy
  • Excellent knowledge of both spoken and written English




  • Verify and make sure that only standardized quality developments, dossiers and registrations with qualified clinical studies are procured and are suitable for the purpose of applying for registrations in the countries of interest and allowing for global marketing
  • Taking into account the pharmaceutical legislation when in assessment of the licenses offered for pharma, biopharma, pharmacokinetic, toxicological and clinical aspects
  • Creation of clinical strategies for early-stage licensed products, ensuring that costs are evaluated as well as risks, inclusive of the creation of a timeline for the product
  • Remain the contact point for the business development and licenses department
  • Make certain timely planning, execution and reporting of pre-clinical and clinical trials/ tests with their risks are in accordance with our clients processes, the applicable regulatory requirements and GxP guidelines



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Contact Information:

Address:  Head Office
Rowan House Smallfield Road Horley Surrey
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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