have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications more »
medical qualification or PhD in a topic relevant to the position is beneficial. Experience working in a clinical drug development environment. Previous experience in pharmacovigilance, including advanced knowledge of PV regulation and cross-functional working. Strong knowledge of international pharmacovigilance requirements, specifically in the UK, Europe and US Salary and more »
have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications more »
have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications more »
gain further experience in the multi-disciplinary management of cancer patients. The activity within the Unit will support training in drug development, study design, pharmacovigilance, project management, and conduct of clinical trials, as well as regulatory aspects of clinical experimentation. Access to an ePortfolio will be facilitated for post holder … gain further experience in the multi-disciplinary management of cancer patients. The activity within the Unit will support training in drug development, study design, pharmacovigilance, project management, and conduct of clinical trials, as well as regulatory aspects of clinical experimentation. Access to an ePortfolio will be facilitated for post holders more »
inform decision-making and drive innovation. Compliance and Regulatory Oversight: Ensure all medical affairs activities comply with relevant regulations, guidelines, and ethical standards, including pharmacovigilance, medical information, and promotional practices, and provide strategic guidance on regulatory submissions and compliance initiatives. Requirements: Education: Advanced degree in life sciences (MD, PharmD, PhD more »
at Cpl Life Sciences (previously Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities. #J-18808-Ljbffr more »
at Cpl Life Sciences (previously Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities. #J-18808-Ljbffr more »
their complex business challenges. As part of the team, you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management. What You'll Do Lead multiple project engagement teams empowering the team to plan and manage all aspects of more »
Hatfield, Hertfordshire, United Kingdom Hybrid / WFH Options
Confidential
leads, and partakes in Eisai Business initiated projects and other ad hoc activities where required. What are we looking for? Demonstrated experience in a Pharmacovigilance role. Prior experience with SDEAs and building relationships with PV partners. In depth knowledge of Pharmacovigilance regulatory reporting requirements in European countries Graduate level education more »
achievements in safety (ex. supporting an ISS responsible for CSR content) Demonstrated experience in specialty TAs incorporating advanced therapies, such as gene therapy into pharmacovigilance practices Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial more »
have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications more »
top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance).As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R&D) space – managing teams more »
