Market Access Lead

Highly Competitive
  1. Permanent
  2. Commercial Operations
  3. United Kingdom
Berkshire, England
Posting date: 07 May 2020
This vacancy has now expired

Proclinical are excited to announce a vacancy for a Market Access Lead to join a pharmaceutical company based in South East England. This organisation is dedicated to discovering and developing treatments that transform the lives of people living with neurological and immunological conditions.

Job Responsibilities

  • Review, extract and accurately enter data from ICSR reports from investigational products.
  • Interpret case-related information including medical conditions, lab results and procedures, as well as compile complete narrative summaries.
  • Review and verify follow-up information for cases and make accurate determination of significant information.
  • Have solid working knowledge of protocol design and details relating to the extraction and entry of SAE from clinical trials reports.
  • Will have data review responsibility, to ensure data entries made by Safety Coordinators are accurate.
  • Will interact with other PVE functional areas to process adverse events efficiently and reliably.
  • Participate in some clinical trial activities with supervision from Manager or Sr Safety Specialist (i.e., protocol
  • May assists in the development of pharmacovigilance presentation for investigator meeting presentations
  • May assist with analysis and evaluation of performance and development of ongoing training for Operations group.

Skills and Requirements

  • 2+years of pharmacovigilance experience and a BS degree in a life sciences field
  • 3+ years of experience in the pharmacovigilance field and an AA degree preferred
  • Healthcare professional degree (i.e., RN, PharmD) and little to no pharmacovigilance experience or industry experience
  • Excellent interpersonal and communication skills, both written and oral
  • Excellent computer skills in Microsoft environment (Microsoft Excel, Power point and Word).
  • The ability to assess data and understand the medical/safety implications
  • Knowledge and experience with safety reporting and regulatory compliance and experience with international safety reporting/regulations is preferred
  • Demonstrated success working both independently and in collaboration with others

To Apply

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Harry Williams on +44 203 854 0102 or upload your CV on our website -

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.