DRUG SAFETY AND MEDICAL jobs in CAMBRIDGE, United Kingdom

experience working with drug safety / PV or related systems, databases, and tools. Strong analytical thinking skills.... Job Description Manager, Quality Management within Strategic Operations, Patient Safety The Patient Safety (PS) department is a global...

strategic direction within drug safety and to the development of safety standards and processes. Key Accountabilities: In... collaboration with the Director of Drug Safety, participate in monitoring, review, analyses, interpretation and evaluation...

. Experience working with drug safety / PV or related systems, databases, and tools. Strong communication and writing skills.... Job Description Senior Specialist, Quality Management within Strategic Operations, Patient Safety The Patient Safety (PS) department...

of senior management key pharmacovigilance findings Provides global medical leadership for product-focused safety activities..., and supports management of any potential safety issues Essential Duties: Oversees clinical development and medical safety...

. Coaches others leaders in resolving problems. Partners with stakeholders to implement and support drug safety computerized...’ relevant experience. BA/BS with 10+ years’ relevant experience. Extensive drug safety or related experience in the biopharma...

possible, together. Job Description FUNCTION: Inflammation Therapeutic Area (TA) Global Safety Leader POSITION OVERVIEW: The... RESPONSIBILITIES: Serves on cross-functional Global Development Teams as the safety expert, go-to-person, for safety profile...

possible, together. Job Description FUNCTION: Medical Safety Science (MSS) / Global Therapeutic Area (TA) Safety Scientists... teams. May serve as medical monitor for post-authorization safety studies. May have one or more direct reports...

Job Purpose The Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development...: Managing and providing scientific contribution to the preparation, editing and review of medical, regulatory and clinical...

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical.... Key Accountabilities: Lead scientific contribution to the development of medical, regulatory and clinical documents...

Responsibilities: Provides medical oversight of outsourced study conduct including interactions with CRO medical and drug safety... closely with the Drug Safety Officer to support overall surveillance of safety activities related to MoonLake clinical...

. You will be responsible for overseeing contract lab testing and supporting safety testing for novel drug products targeting oncological... the establishment of rapid microbial method testing for lot release of drug product to support internal clinical...

clinical performance, effectiveness, or safety of Software as a Medical Device (SaMD). You have a Bachelor’s or advanced... Clinical Operations function of Clinical and Medical Affairs. Support, update, and maintain the Clinical Trial Management...

protection and data exclusivity. In collaboration with other GMRS functions ensure the establishment of CCDS and required safety... experience of drug development and managing complex worldwide products/projects within a relevant therapeutic area, in key...

medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity... for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to support drug development...

and other stakeholders, as well as to avoid errors in product information labeling to protect patient safety. RO LAT works closely with cross... submission team meetings, and on joint labeling/safety meetings with partner companies. You will act as the main point...

transformational medicines to those in the “International region” with continued unmet medical need. This is an exciting opportunity... for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to support drug development...

and required safety plans for the assigned product. Ensure regional regulatory specificities and needs are incorporated into the global... with Ipsen’s ethics and compliance policies Knowledge, abilities & experience: Ideal Proven experience of drug development...