Safety Data Associate
7 days ago
We are seeking a highly organized and detail-oriented Pharmacovigilance Data Associate to support our team at EPM Scientific. The successful candidate will be responsible for assisting in case processing and MedDRA coding of safety events, data entry in the Pharmacovigilance Database, and monitoring adverse events.
Responsibilities:
- Assist in case processing and MedDRA coding of safety events
- Data entry in the Pharmacovigilance Database
- Maintain the Pharmacovigilance Database
- Monitor adverse events (AEs) arriving via EEDR
- Produce safety data for signal detection and periodic aggregate reports
- Provide safety data for regulatory submissions
Requirements:
- Life science degree required
- Working knowledge of GVP and ICH GCP guidelines
- At least 3 years' experience in pharmacovigilance compliance/quality fields
- Excellent attention to detail and computer literacy
- Ability to plan, organize and follow up on tasks
- Maintain current awareness of pharmacovigilance requirements
- Effective verbal and written communication skills
- Teamwork and problem-solving skills
- Inquisitive mind and effective time management
What We Offer:
- A competitive salary with benefits package of £40,000-£55,000 per annum
- The opportunity to contribute to a team making a positive impact on healthcare
- A hands-on role with commercial exposure
- The chance to work with world-leading scientific experts
- A collaborative environment with talented colleagues
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