Global Pharmacovigilance Specialist

Job SummaryAs a Global Pharmacovigilance Coordinator at Medpace, you will be responsible for coordinating pharmacovigilance activities across multiple regions.Key ResponsibilitiesCollaborate with cross-functional teams to ensure compliance with regulatory requirementsDevelop and maintain safety databases and associated documentationCoordinate safety-related...

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...

Job SummaryAt Medpace, we are seeking a highly motivated Pharmacovigilance Specialist to join our Clinical Safety team in Stirling. As part of a high-performing group, this position plays a key role in accomplishing tasks and working on projects that contribute to the development of life-changing medicines. The successful candidate will be responsible for...

Key ResponsibilitiesWe are seeking a highly skilled Pharmacovigilance Team Member to join our Clinical Safety team in Stirling.You will work closely with Medical Monitors, Quality Assurance, and other teams to ensure the safe development of medicines.Collect, process, and track SAE reports to identify potential safety signals.Generate safety narratives and...

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 DescriptionIn this role, you will collect, process, and track serious adverse event reports to support the development of life-changing medicines.Main ResponsibilitiesCollect, process, and track SAE reports.Generate safety narratives and queries.Perform quality control of safety cases.Prepare clinical safety documents.Attend internal and external...

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 -...

Job Description:The Global Adverse Event Manager will be responsible for overseeing the collection, processing, and tracking of adverse event reports in clinical trials. This includes generating safety narratives and queries, performing quality control of safety cases, and preparing clinical safety documents.Duties and Responsibilities:Manage and monitor...

Clinical Safety Specialist Job Summary:We are seeking a skilled Clinical Safety Specialist to join our team in Stirling. As a key member of our Clinical Safety group, you will work closely with Medical Monitors, Quality Assurance, and Clinical Trial Management to ensure the timely collection, processing, and tracking of SAE reports.Key...

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...

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...

About the Role:We are seeking a highly motivated Clinical Safety Specialist to join our European Pharmacovigilance team in Stirling. As a key member of our Clinical Safety group, you will work closely with Medical Monitors, Quality Assurance, and Clinical Trial Management to ensure the timely collection, processing, and tracking of serious adverse event...

Job Overview:We are looking for an experienced Pharmacovigilance Specialist to join our UK team at Medpace. The successful candidate will play a key role in ensuring compliance with global clinical safety regulatory requirements.Main Responsibilities:Manage clinical safety activities and multiple large programs.Develop and maintain safety management...

Job DescriptionWe are looking for a Global Safety Operations Manager to join our UK team in Stirling. The successful candidate will be responsible for managing clinical safety activities and multiple large programs, as well as providing expert safety knowledge to clients and internal stakeholders.Key Responsibilities:Manage Clinical Safety activities and...

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 -...

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...

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...

About the JobEstimated Salary: £60,000 - £80,000 per annum.We are looking for a talented Video Production Specialist to join our team at Global Voices Ltd. The ideal candidate will have experience in creating engaging video content that meets our business objectives and resonates with our global audience.Develop and implement a content strategy that aligns...

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...