Affiliate Pharmacovigilance Compliance Specialist

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and...

A leading pharmaceutical company seeks a Case Management Specialist for a 12-month student placement in Maidenhead. You will manage incoming safety information and collaborate on various projects within the Pharmacovigilance division. This role offers high exposure in drug development and requires completion of a science degree with a focus on accuracy and...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

LMS Case Management Specialist - Student Placement Position: Student Placement | Company: Johnson & Johnson Innovative Medicine Job Function: Career ProgramsJob Sub Function: Non-LDP Intern/Co-OpJob Category: Career ProgramLocation: High Wycombe, Buckinghamshire (Moving to Maidenhead in Oct 2026)Duration: 12 months Overview LMS Case Management Specialists...

The IPV Training Specialist as a member of the International Pharmacovigilance (IPV) group supports support the delivery of high-quality Pharmacovigilance services by coordinating, delivering, and tracking training to employees, Distributors (InternationalPartner Markets), and contracted Vendors. Training will include new employee on-boarding, program...

A multinational pharmaceutical company is seeking a LMS Case Management Specialist for a student placement. This role involves collecting and evaluating information regarding medicine usage and side effects. The ideal candidate will have completed two years of a science degree and will be proactive with excellent communication skills. Responsibilities...

A global biotherapeutics leader based in Maidenhead is seeking an experienced professional for an operational role handling pharmacovigilance and regulatory affairs. You will manage platform implementations, ensuring safety compliance and optimizing processes in alignment with global standards. The ideal candidate has at least 12 years of experience in the...

The position is part of a team responsible for continuous analysis of global documents and regulatory intelligence from interface functions to decide on relevant updates to regulatory and business reporting requirements.This position is to be based onsite (hybrid working) in Maidehead UU, Zurich CH, or King of Prussia (US)Key ResponsibilitiesOversee...

Global Regulatory Affairs Manager – International Growth Markets (IGM) – contract jobYour newpany Are you a strategic regulatory professional ready to make a global impact? Our client, a leading pharmaceuticalpany, is seeking a Global Regulatory Affairs Manager to join their high-performing team. This is a unique opportunity to shape regulatory...

The position is part of a team responsible for continuous analysis of global documents and regulatory intelligence from interface functions to decide on relevant updates to regulatory and business reporting requirements. This position is to be based onsite (hybrid working) in Maidehead UU, Zurich CH, or King of Prussia (US) Key Responsibilities Oversee...