Department:517050 Medical Writing - TTIL Location:San Diego, United Kingdom - Remote, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.
The Role This a portfolio-level regulatory strategy role covering regions with diverse regulatory requirements and market dynamics: APAC, LATAM, MEA, CIS, Adriatics and Partner Business Regions. Working with the Therapeutic Area Lead, youll set regional regulatory
About This Role: As a Senior Pharmacovigilance (PV) Scientist, you will play a pivotal role as a product lead within the Safety team, overseeing and spearheading critical PV activities. Your responsibilities encompass managing the safety signal
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Description Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across
Meet Life Sciences is seeking a Director, Medical Safety Physician Product Lead to provide medical leadership for global pharmacovigilance efforts across product lifecycles. The role encompasses benefit-risk assessment, signal detection, safety surveillance, and regulatory safety strategy,
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director to join our Patient Safety team. The Executive Director, Global
Director, Pharmacovigilance Hybrid. Full time. Location: London, UK / Hybrid Reporting to: VP Pharmacovigilance Job Summary The Director, Pharmacovigilance is a safety expert with medical/scientific knowledge on the safety and benefit‑risk profile of one or more
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Regulatory Affairs Coordinator Hertford Hybrid/Part-Time Working Available Up to £40,000 An established manufacturer of regulated products is seeking a Regulatory Affairs Coordinator to support the ongoing maintenance of compliance and technical documentation across an established portfolio
Viatris is seeking a Director of Safety Surveillance & Risk Management for a 12-month fixed-term contract at Hatfield, UK. You will lead global pharmacovigilance activities, act as a medical safety expert, and drive PSUR/RMP processes in line
At Gilead, were creating a healthier world for all people. For more than 35 years, weve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives
We are seeking a Regulatory Affairs Manager to join our global team based in Hampshire, UK. The Regulatory Affairs Manager role offers you an exciting opportunity to join our highly motivated Product Development – Injectables team,
Job Title Medical Director, Senior Patient Safety Physician Location 3 days onsite in Luton, UK Key Responsibilities Develop and implement the Clinical Safety strategy for assigned drug projects and products throughout all stages of development and
PrecisionLife is helping transform the delivery of healthcare by building the next generation of precision medicine solutions and Mechanostics® tests to improve disease detection, patient triage & outcomes, predict patients’ drug responses, and reduce the cost
Senior Regulatory Affairs Specialist - (12‑Month Contract) / London (Hybrid) Our client, a leading pharmaceutical organisation specialising in Dermatology, is seeking an experienced Senior Regulatory Affairs Specialist to support UK & Ireland regulatory activities across medicinal
The Role This a portfolio-level regulatory strategy role covering regions with diverse regulatory requirements and market dynamics: APAC, LATAM, MEA, CIS, Adriatics and Partner Business Regions. Working with the Therapeutic Area Lead, youll set regional regulatory
Company: Ipsen Pharma (SAS) Location: Paris, London (UK) Time Type: Full time Job Requisition ID: R-22023 About Ipsen Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology,
Madrid, Spain Reading, Berkshire, United Kingdom Dublin, Ireland Full time R Senior Global Trial Manager - Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a