Adverse Event Specialist

3 weeks ago


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

CK Group is seeking a Pharmacovigilance Associate to join a prominent global pharmaceutical organization on a contract basis. This role is designed for individuals looking to contribute to patient safety and drug monitoring initiatives.

Compensation:

£20.00 per hour PAYE

Key Responsibilities:
  • Oversee the collection and assessment of Individual Case Safety Reports (ICSRs) and Serious Adverse Events (SAEs) related to both marketed and investigational products, ensuring compliance with local and EU regulations.
  • Assist in the submission of Teva UK/IE ICSRs to the European Hub.
  • Input ICSRs and SAEs into the V-Safe system as necessary.
  • Draft follow-up correspondence, including letters and emails.
  • Provide support to the case management team with various tasks as needed.
Candidate Profile:
  • Basic understanding of pharmacovigilance principles.
  • Effective verbal and written communication skills in English.
  • Strong organizational abilities.
  • Customer-focused mindset, both internally and externally.
  • Meticulous attention to detail.
  • A collaborative team player.
  • Proficient in Microsoft Office applications.
Company Overview:

Our client is dedicated to becoming a global leader in generics and biopharmaceuticals, with a mission to enhance the quality of life for patients worldwide.

Work Arrangement:

This position involves a hybrid work model, requiring attendance at the client’s site for two days each week, with the remaining three days available for remote work.

Application Requirements:

Applicants must possess the legal 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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