Adverse Event Analyst

4 weeks ago

Harlow, Essex, United Kingdom CK Group Full time
Position Overview:

CK Group is seeking a dedicated Pharmacovigilance Associate to join a leading global pharmaceutical organization on a contract basis. This role will primarily focus on the management of safety reports related to both marketed and investigational products.

Key Responsibilities:
  • Oversee the receipt and evaluation of Individual Case Safety Reports (ICSRs) and Serious Adverse Events (SAEs) in compliance with local and EU regulations.
  • Assist in the submission of ICSRs to the EU Hub.
  • Input ICSRs and SAEs into the V-Safe system as necessary.
  • Draft follow-up correspondence, including letters and emails.
  • Support the case management team with various tasks as needed.
Candidate Profile:
  • Basic understanding of pharmacovigilance principles.
  • Excellent verbal and written communication skills in English.
  • Strong organizational abilities.
  • Customer-focused mindset.
  • Meticulous attention to detail.
  • A collaborative team player.
  • Proficient in Microsoft Office applications.
Company Overview:

Our client is committed to becoming a global leader in generics and biopharmaceuticals, enhancing patient outcomes worldwide.

Work Arrangement:

This position offers a hybrid work model, requiring presence at the client's site for part of the week while allowing remote work for the remainder.

Application Requirements:

Applicants must have the right to work in the UK. Please reference the job title in all communications.

Note:

This position may require a satisfactory basic Disclosure and Barring Service (DBS) check.

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