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Posts Tagged ‘Drug Safety Recruitment’

Drug Safety Associate based in Buckinghamshire, UK

Monday, January 18th, 2010

Drug Safety Associate based in Buckinghamshire, UK

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Our client, a  leading pharmaceutical company, are currently recruiting for a Drug Safety Associate to join their team based in Buckinghamshire, on a contract basis. You will responsible for the receipt and data entry of adverse event reports following Company Standard Operating Procedures, internal business practices and regulatory guidance documents to ensure compliance with worldwide safety regulations and corporate policies. Previous case processing experience is required.

Key responsibilities of this Drug Safety Associate role include:

  • Triage of incoming cases to determine seriousness for prioritisation of daily workflow.
  • Confirmation of Safety Co-ordinator case registry data.
  • Database searches as necessary.
  • Completion of literature searches as necessary.
  • Completion of remaining case data entry, including narrative or auto-narrative.
  • Completion of risk and quality (label, approval, manual coding & quality review steps.
  • Clarification of unclear or illegible information from the LSO or Call Centre.
  • Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician.
  • Completion of protocol request forms as necessary.
  • Preparation of deviation memo as necessary.
  • Request deletions as necessary.
  • Single case unblinding.
  • Understand relevant safety implications regarding contracts with operating companies and/or marketing partners.
  • Review and make suggestions for system and procedure enhancements.
  • Participation in inspections and audits, as required.
  • Participation in local or global project teams.

This position is to work on a oncology drug, therefore experience in oncology and the Argus database is a bonus to hit the ground running (but not essential).

  • Candidates must have a Life Science degree or be a qualified nurse.
  • Pharmacists are not suited unless they have recent experience in Drug Safety.
  • Reasonably local people are preferred.

Successful candidates will enjoy the benefits of working with a global Pharmaceutical company, including a competitive rate as well as ongoing professional development.

If you would like to hear more about this Drug Safety Associate role, please contact Hendre on Tel: +44 (0)1438 870 023 or email me at hmoolman@ckclinical.co.uk quoting 19124 to indicate your interest.

Apply for this Drug Safety Associate job now.

Keywords: Drug Safety Officer, Pharmacovigilance Officer, Drug Safety Associate, Pharmacovigilance Associate, Contract, Argus, Life Science, Literature, Case processing.

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. 

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Senior Data Associate, Drug Safety – South East, UK

Monday, December 14th, 2009

Our client, a global leader in the commercialization of pioneering therapies, are currently seeking an experienced Senior Data Associate to join their team in the South East of England.

Working as a Senior Data Associate in Drug Safety you will be responsible for the following:

  • Adverse Event case management:          
    • Initial assessment and classification.
    • Perform follow-up review and close individual case safety reports.
    • Review case narratives.
    • Facilitate and ensure medical review of all adverse events from clinical trials and commercial use.
  • Participating in Pharmacovigilance reviews, identify/collate adverse event case series, assist in event signaling.
  • Identifying expedited reports and ensuring their timely evaluation and preparation for submission to regulatory authorities. 
  • Participating in PSUR preparation. 
  • Participating in the Post marketing and Clinical Trial Case Review Meetings.
  • Ongoing identification and implementation of safety process refinements.
  • Performing other duties as requested by Pharmacovigilance management.

The successful candidate will be educated to a minimum degree level in Biomedical Science, Pharmacy or Nursing and will have previous experience in Drug Safety and Clinical Trials. It is also essential that you have previous working experience in post marketing drug safety, clinical trial safety and pharmacovigilance.

This is a fantastic opportunity for an experienced Senior Data Associate to assist this global pharmaceutical company to meet the unmet medical needs of patients in more than 90 countries.

If you would like more information about this role, please contact Hendre Moolman on 01432 743047 or email hmoolman@ckclinical.co.uk. Alternatively, to apply, click here.

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry. 

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PIPA Conference 2009 – Thank you

Monday, July 13th, 2009

Following a successful PIPA Conference 2009, the pharmacovigilance recruitment team would like to thank Ann and Sharon for arranging such a good conference.

Year in and year out the PIPA conference is always welcoming and a valuable networking opportunity for the CK Clinical Medical information recruitment and drug safety recruitment team and this year was no exception.

The conference gave us the opportunity to pick up new medical information jobs from some of our valued customers that we have worked with for years as well as develop relationships with some new customers to help them recruit for their drug safety jobs. We look forward to working with you

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