Global Adverse Event Coordinator

6 hours ago


Stirling, Stirling, United Kingdom Bancroft School Full time

Medpace is seeking a skilled Global Adverse Event Coordinator to join our Clinical Safety team in Stirling, Scotland. As a key member of our team, you will play a vital role in ensuring the safe conduct of clinical trials by identifying and managing potential risks associated with investigational products.

The estimated salary for this position is £35,000 - £55,000 per annum, depending on experience. This is a full-time role with hybrid work-from-home options and a competitive benefits package.

Your responsibilities will include collecting, processing, and tracking serious adverse event (SAE) reports, generating safety narratives and queries, and performing quality control of safety cases. You will also be involved in data entry into safety databases and reconciling SAEs between safety and clinical databases. Additionally, you will prepare clinical safety documents and attend internal and external meetings as required.

You will have the opportunity to lead clinical trial projects, develop presentation materials for Sponsor meetings, and coordinate final medical review of study report narratives. Your expertise in safety reporting requirements and Good Clinical Practice (GCP) guidelines will be essential in ensuring compliance with regulatory requirements.

We are looking for a highly motivated individual with a minimum Bachelor's degree in life sciences and 2+ years of experience in clinical trial pharmacovigilance. You should have a working knowledge of safety databases and demonstrate advanced knowledge of medical terminology and global safety reporting requirements. Exposure to working on global trials as part of a multidisciplinary team is also desirable.

As a valued member of our team, you will enjoy a range of benefits including competitive compensation, flexible work schedules, and opportunities for professional growth and development. If you are passionate about ensuring patient safety and have a strong background in clinical pharmacovigilance, we encourage you to apply for this exciting opportunity.



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