Clinical Safety Associate

As a Senior Drug Safety Associate at ICON, you will be part of a global team dedicated to ensuring the safety of patients and healthcare professionals. Your primary responsibility will be to receive, process, and manage individual case safety reports (ICSRs) from clinical trials, spontaneous reports, and published literature.Key Responsibilities:Track and...

Job SummaryAs a Senior Drug Safety Associate, you will be part of a dynamic team at ICON, working on clinical research projects that make a real difference in people's lives. Your primary responsibility will be to receive, process, and analyze individual case safety reports (ICSRs) from clinical trials, spontaneous reports, and published literature. This...

As a key member of the ICON team, you will be responsible for overseeing the conduct of clinical trials in a pharmaceutical or biotechnology company. Your role will involve partnering with project managers to implement study plans and ensuring the timely submission of protocols and safety reports.Main Responsibilities:Coordinate and advise others on all...

As a Senior Drug Safety Associate, you will be joining the world's largest and most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people's lives. Working in this program, you will feel...

As a Senior Drug Safety Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people's lives. Working in this program you will feel...

As a Senior Drug Safety Associate at ENGINEERINGUK, you will be part of a world-class team that is dedicated to ensuring the safety of patients and advancing the field of pharmacovigilance.Key Responsibilities:Process and analyze individual case safety reports (ICSRs) from clinical trials, spontaneous reports, and published reports.Perform coding of...

As a key member of the ICON team, you will be responsible for the conduct and management of clinical trials. This will involve ensuring the accuracy and completeness of data entered into systems, participating in training and mentoring new staff, and conducting regular monitoring visits in accordance with ICON's site monitoring SOP.You will be working...

Role OverviewThis role is an excellent opportunity for a skilled Clinical Safety Professional to partner with a leading pharmaceutical company, ICON, in improving and saving lives through pharmacovigilance.Key ResponsibilitiesReceive and process individual case safety reports (ICSR) from clinical trials, spontaneous, and published reports, ensuring timely...

As a Senior Drug Safety Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged...

As a Senior Clinical Research Associate at ENGINEERINGUK, you will be part of the world's largest and most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people's lives. Working in this program, you...

Health and Safety Associate RoleWe are seeking a skilled Health and Safety Associate to support our Subsidiary Management and Corporate Governance team. As a key member, you will provide administrative assistance, ensuring compliance with relevant regulations, maintaining safety records, and assisting in the implementation of safety programs and procedures...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet...

As a Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will be part of an innovative and global Biotechnology company, which prides itself on being one of the world's leading independent biotechnology companies. They focus on areas with...

Sr Centralized Study Associate Fortrea Inc. is seeking a dedicated professional to support the success of our clinical studies. As a Clinical Study Associate, you will be responsible for: Clinical Systems & Access Management: Managing clinical systems and access. Maintaining study databases (CTMS, IWRS, EDC, etc.). Supporting the study team in data...

At ICON, we're a global leader in clinical research, and as a Clinical Research Associate - Regulatory Compliance Specialist, you'll play a vital role in ensuring the integrity of our studies.We're looking for an experienced professional to join our team and support our oncology projects. The ideal candidate will have at least 2 years of on-site monitoring...

As a Clinical Research Associate, you will be joining the world’s largest and most comprehensive clinical research organisation, powered by healthcare intelligence. You will be part of an innovative and global biotechnology company, which prides itself on being one of the world's leading independent biotechnology companies. They focus on areas with...

Role Summary:As a Senior Safety Specialist at ENGINEERINGUK, you will be part of a world-class team dedicated to the discovery and development of life-changing treatments.You will be working closely with a leading pharmaceutical company to identify and mitigate potential safety risks associated with their products.Key Responsibilities:Receive and process...

At ENGINEERINGUK, we're looking for an experienced Clinical Research Associate to join our team in a challenging and rewarding role. As a key member of our global clinical research organization, you will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and working closely with our biotechnology clients.About...

About the RoleWe are seeking a highly skilled and motivated Clinical Research Associate Manager to join our team at Fortrea Inc. In this role, you will be responsible for managing clinical systems, study databases, and data review, as well as tracking and following up with CRAs for outstanding issues.Key ResponsibilitiesClinical Systems & Access...

Role SummaryThis role will have you working in the world's largest and most comprehensive clinical research organisation, powered by healthcare intelligence.You will be partnering with a pharmaceutical company dedicated to discovering and developing treatments that improve and save people's lives. You will feel challenged and supported to advance in your...