Job Description Evolve have partnered with a global pharmaceutical company specialising in generics who are seeking a Pharmacovigilance Associate. This Gloucestershire office-based role offers the opportunity to take ownership of global safety data and key business partnerships, while supporting wider medical affairs activities. With strong development support and flexibility to grow the role,...
Pharmacovigilance Associate (Office based) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team....
Pharmacovigilance Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a...
Evolve have partnered with a global pharmaceutical company specialising in generics who are seeking a Pharmacovigilance Associate. This Gloucestershire office-based role offers the opportunity to take ownership of global safety data and key business partnerships, while supporting wider medical affairs activities.With strong development support and flexibility to grow the role, this is an...
Overview CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products. As a Safety Scientist, you key responsibilities will...
Quality Associate (full time) - Permanent, Milton Keynes Salary 28-35K DOE Our client is a market leader within the Pharmacovigilance sector They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years’ experience...
Job Description Quality Associate (full time) - Permanent, Milton Keynes Salary 28-35K DOE Our client is a market leader within the Pharmacovigilance sector They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2...
Senior Pharmacovigilance Manager – Biopharmaceuticals - Hertfordshire / Remote Our client, a global biopharmaceutical company with plants across Europe and North America is looking for a Senior Pharmacovigilance Manager to join their team in the UK. This is your chance to be part of one of the top players in the field of plasma-derived products, supplying high-quality medicines treating rare...
Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned well for an exciting future of continued...
Job Description Location: South West Region UK Make an impact on global health by driving high-quality clinical research. In this role, you’ll be the primary site contact and operational lead across all phases of clinical trials—ensuring excellence in performance, compliance, and patient safety. Under the guidance of the CRA Manager, you’ll own your sites end-to-end, build strong relationships,...
Location: South West Region UK Make an impact on global health by driving high-quality clinical research. In this role, you’ll be the primary site contact and operational lead across all phases of clinical trials—ensuring excellence in performance, compliance, and patient safety. Under the guidance of the CRA Manager, you’ll own your sites end-to-end, build strong relationships, and help expand...
You will analyze interesting problems, build insightful solutions, and develop close working relationships with stakeholders to deliver realizable value, at the forefront of digital and R&D innovation. Opportunities are available across Europe for this role as this is a remote position.
Job descriptionSite Name: UK London New Oxford StreetPosted Date: Jan 2 2026This is an individual contributor position in the HIV Therapeutic Area and will serve as Safety Lead for a product.Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) group and defining and driving the strategy and vision of clinical safety and pharmacovigilance...
This is an individual contributor position in the HIV Therapeutic Area and will serve as Safety Lead for a product.Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) group and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies.As a senior member of...
Quality Associate (full time) - Permanent, Milton Keynes Salary 28-35K DOE Our client is a market leader within the Pharmacovigilance sector They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years’ experience...
Location: South West Region UK Make an impact on global health by driving high-quality clinical research. In this role, you’ll be the primary site contact and operational lead across all phases of clinical trials—ensuring excellence in performance, compliance, and patient safety. Under the guidance of the CRA Manager, you’ll own your sites end-to-end, build strong relationships, and help expand...
You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through face-to-face discussions, workshops, email, etc.) to deliver demonstrable, sustainable value, at the forefront of digital and R&D innovation. Opportunities are available across Europe for this role as this is a remote position.
Quality Associate (full time) - Permanent, Milton Keynes Salary 28-35K DOE Our client is a market leader within the Pharmacovigilance sector They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years’ experience...
South West Region UK Make an impact on global health by driving high-quality clinical research. In this role, you’ll be the primary site contact and operational lead across all phases of clinical trials—ensuring excellence in performance, compliance, and patient safety. Under the guidance of the CRA Manager, you’ll own your sites end-to-end, build strong relationships, and help expand our...
Quality Associate (full time) - Permanent, Milton Keynes Salary 28-35K DOE Our client is a market leader within the Pharmacovigilance sector They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years’ experience in...