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East Sussex, Kent, Oxfordshire, Surrey, West Sussex, Middlesex, London - East, London - South
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
16 May 2008
An opportunity has come up with a TOP global pharma company to work with in Drug Safety. This is an excellent chance for someone looking to enter into the pharmacovigilance sector and offers some fantastic prospects for progression in the future.
The role will be responsible for the accurate data entry of Serious Adverse Event / Post Marketing Adverse Event and the evaluation of non-expeditable reports within agreed timeframes, in compliance with CS&E business rules, standard operating procedures and regulatory requirements.
Major Activities:
1. Accurate and consistent data entry of Serious Adverse Event / Post Marketing Adverse Event from source documents with emphasis on timeliness and quality.
2. Evaluation and processing of non-expeditable AEs reports.
3. Use thesauri and working practice documents to code medical history, drugs and adverse event terms. Prepare event narratives summarizing the essential details of the case. Assess each report to determine the necessity for follow-up and prepare follow-up request as needed.
4. Work in conjunction with Clinical Safety Scientists and Medical Safety Experts to ensure that reports are accurately evaluated and databased
5. Assist Clinical Safety Scientists with administrative and procedural activities within specific therapeutic areas
Requirements:
Life sciences qualification/degree / Nursing
Good knowledge/fluency in English. Knowledge of other languages desirable.
Previous safety or clinical trial experience desirable, but not essential
Previous data entry experience desirable, but not essential
Familiarity with medical terminology and working with databases
Keywords - Clinical Safety Associate South East
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