Pharmacovigilance Lead

Are you a skilled professional looking for a challenging role in clinical pharmacovigilance? We are seeking an experienced Clinical Pharmacovigilance Specialist to join our team at Medpace in Stirling, Scotland. As a key member of our Clinical Safety department, you will play a vital role in ensuring the safety of patients participating in clinical...

Job Overview: Medpace, Inc. is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. As a Global Pharmacovigilance Coordinator, you will play a critical role in accelerating the global development of safe and effective medical...

We are seeking a highly skilled Senior Safety Professional to join our Clinical Safety team at Medpace in Stirling, Scotland. In this role, you will play a critical part in ensuring the safe conduct of clinical trials by identifying and mitigating potential risks associated with investigational products.The estimated salary for this position is £50,000 -...

Medpace, Inc. is a leading contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.About the Job:This Clinical Safety Professional will be responsible for managing clinical safety activities, maintaining relationships with clients, and overseeing clinical...

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 -...

About the Role: Medpace, Inc. is seeking a skilled Clinical Safety Specialist to join its European Pharmacovigilance team in Stirling. The successful candidate will be responsible for collecting, processing, and tracking serious adverse event reports.Main Responsibilities:Generate safety narratives and queries.Safety Database data entry.Perform quality...

MEDPACE is a leading CRO providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.About the RoleWe are looking for a highly skilled Clinical Safety Manager to lead our pharmacovigilance team and manage multiple large clinical safety programs. The ideal candidate will have a strong background in...

Company Overview: Medpace, Inc. is a leading clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With a focus on accelerating the global development of safe and effective medical therapeutics, we are committed to delivering high-quality results...