Pharmacovigilance Manager

MEDPACE, a full-service CRO, is seeking an experienced Clinical Safety Manager to lead our pharmacovigilance team.About the JobThe successful candidate will have a strong background in clinical safety and project management, with experience in managing multiple large clinical safety programs. They will be responsible for developing and implementing safety...

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...

Job DescriptionWe are seeking a skilled Clinical Safety Specialist to join our Pharmacovigilance team at Medpace in Stirling. In this role, you will work closely with cross-functional teams to collect, process, and track serious adverse event reports, generate safety narratives and queries, and perform Safety Database data entry, quality control review, and...

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...

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...

Job OverviewThis role involves collecting, processing, and tracking serious adverse event reports to support the development of life-changing medicines.ResponsibilitiesCollect, process, and track SAE reports for the development of life-changing medicines.Generate safety narratives and queries to ensure compliance with GCP Guidelines.Perform quality control...

We are seeking an experienced Clinical Safety Professional to join our UK team at Medpace, Inc. as a full-time, office-based employee.About the Role:This position plays a pivotal role in the pharmacovigilance process and works collaboratively with the team to accomplish tasks and projects instrumental to the company's success.Key Responsibilities:Manage...

Join us as a Quality Officer **Hours**: 35 Hours per Week - Monday to Friday 9am to 5pm **Location**: Stirling **Start date**: ASAP **The role (in a nutshell)** Assistance in administration of the Quality Management System and helping ensuring it adheres to all ISO standards. To be involved in the completion of internal audits, maintenance of the...