Your Responsibilities: The successful candidate will be tasked to provide industry leading statistical support of the broader ID clinical development organization.  Candidate qualifications include:  Track record of statistical contrib...

Basic qualifications: MS (with at least 4 years pharmaceutical or biotechnology experience) or Ph.D. (with at least 2-3 years of pharmaceutical or biotechnology experience) in immunology, molecular biology, molecular oncology or pathology. Experie...

Your Responsibilities:  The Medical Director is accountable for the clinical development of one or more assets in Immuno-Oncology (IO), Oncology Cell Therapy (OCT), and Cancer Epigenetics (CE). These three Discovery Performance Units (DPUs) focus on...

Your Responsibilities:  Responsibilities of the role include: • Join a group of innovative statistical scientists working in close collaboration with project teams and key stakeholders to design more effective studies which: raise the likeli...

Basic qualifications:  • DVM or equivalent is required • Veterinary Pathology board certification by ACVP, ECVP, FRCPath, or equivalent is required Preferred qualifications:  N/A Details:  Welcome to the UK/US Path...

Your Responsibilities:  Biology: The field of biology research and development, including imaging science. Biological Sciences: Performs biological discovery and development research  within a major or significant therapeutic area or a sub...

Basic qualifications: M.D., PhD, or MD/PhD degree 10 years pharmaceutical or relevant medical/clinical experience Keen understanding of translational medicine and its role in drug development Experience with translational investigation of cell...

Your Responsibilities:  You will provide matrix leadership of other medical, clinical and/or scientific directors and managers to define the direction, planning, execution, and interpretation of clinical trials or research activities of one or ...

Your Responsibilities:  Responsible for a whole study from design to execution for different study designs. KEY RESPONSIBLITIES - to use stat methodology to establish study strategy (eg  power modelling of different scenari, set up power ...

Your Responsibilities:  The Sr. Manager Molecular Analytics is expected • Lead team of virologists and molecular biologists to design and develop analytic tools and assays for the characterization of vaccine candidates, and support platform tec...

Your Responsibilities:  To conduct Phase I-IV Clinical Development activities within a large program or group of related programs (led by a Clinical and Epidemiology Research & Development Project Lead - CEPL) or, for a mid-size program, to ...

Your Responsibilities:  The employee is part of upstream process development team responsible for the development of early and late phase processes for the production of vaccines; performing cell culture development activities for recombinant vaccin...

Your Responsibilities:  The Study Delivery Lead (SDL) is the single accountable for the execution and the delivery of the study to time, budget and quality as defined in the Development Plans (Clinical, Epidemiology, Global and local studies) ...

Your Responsibilities:  GlaxoSmithKline (GSK) is one of the world’s leading research-based pharmaceutical companies with a broad range of innovative products in three primary areas: Pharmaceuticals, Vaccines and Consumer Healthcare. GSK va...

Your Responsibilities:  As the Director of Biostatistics and Statistical Programming you will have at least 10 years of experience in pharmaceutical products development,  preferably for Vaccines.    You will have been managing...