Senior Pharmacovigilance Officer - clinical trials

Location
Essex (GB)
Salary
Competitive salary and benefits
Posted
11 Sep 2019
Closes
03 Oct 2019
Ref
2103SPVOCT
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

DETAILS:

  • Full-time permanent position
  • Office based in Essex
  • Competitive package

THE JOB:

  • Knowledge and use of the pharmacovigilance database for processing of Serious Adverse Events (SAE) and Serious Adverse Drug Reactions (SADRs).
  • Triage and QC sign-off of AEs, AESIs, SAEs and SADR reports.
  • Testing for electronic submission via EudraVigilance for relevant Health Authorities as required.
  • Submission of SAEs and SADRs in the appropriate format to the Regulatory bodies, in compliance with the statutory timelines.

Full details available on application

THE CANDIDATE:

  • 2 years plus working in clinical trial pharmacovigilance Scientific degree Proficient in the use of Microsoft office applications such as Excel, Word and PowerPoint 
  • Only candidates with existing right to work in the UK/EU will be considered

TO APPLY:

Please complete the details below to apply. For further information or a discreet discussion regarding your recruitment requirements, please call Alex on 01227 844466 or email alex@apexrecruitment.com

To view our other vacancies, please visit our website on www.apexrecruitment.com

Apex Recruitment are a specialist agency providing opportunities within the pharmaceutical, biopharma, biotech and medical device industries recruiting in the areas of medical affairs, drug safety, clinical and quality

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