Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence
Job Level: Senior Director, Drug Development Location: Home-based in Europe Job Overview: Manages a department or small unit.; Provide leadership and advice on the development of optimum regulatory strategies for drug development, IND and marketing approval,
Senior Clinical Data Science Lead At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career
Principal Data Standards Consultant ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission
Medical Director Immunology - Lupus ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our
Job DescriptionIQVIA Biotech has an exciting position within its EU Biostats team. As the Biotech and Emerging Biopharma arm of IQVIA, we continue to grow and win new business. Historically IQVIA Biotech focused on Oncology, Dermatology
The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs)
Job Summary:This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance’s. This position provides this guidance and
Job Level: Senior Director, Drug DevelopmentLocation: Home-based in EuropeJob Overview:Manages a department or small unit.; Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio management to meet
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information,
Who we are For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance
Safety Physician – Director Level Global Development | Rare Disease & Neurology | UK You are a medically trained safety leader who wants to move beyond execution and play a defining role in how development programmes
We are looking for experienced Freelance Medical Writers to support an immediate requirement with a leading international organisation working within the life sciences industry. This opportunity would suit an experienced clinical/regulatory writer who has current availability
Overview As SDTM & CRF Design Lead you will oversee end-to-end SDTM activities on a sponsor-dedicated project. You will manage CRF design from the protocol, validate vendor specifications, and define SDTM specifications across studies. You’ll collaborate
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health
Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence
Frankfurt/Main, Germany | Full time | Hybrid | R The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports
# Head of Patient Science, Instrument Development & Thought LeadershipApplylocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R Join us on our exciting journey! IQVIATM is The Human Data Science CompanyTM,
Overview In this Senior Director role, you will lead strategic drug development activities across discovery to market, guiding portfolio and lifecycle decisions to meet client objectives. You will work with cross-functional teams to shape regulatory, clinical,
Join Rephine Barcelona: Leading Life Sciences Quality Worldwide At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, India, we support