BioSpace

Associate Director, Clinical Research, Value & Evidence Generation, US Medical Join to apply for the Associate Director, Clinical Research, Value & Evidence Generation, US Medical role at BioSpace Job Description This role is based in Lexington, MA, with a hybrid work model. The Associate Director will provide clinical project management and leadership to ensure successful operational execution of US Medical Clinical Research, including MACS and IIR studies. Responsibilities include translating strategy into research plans, managing study design and conduct, overseeing budgets, and leading cross-functional teams to meet project and strategic objectives. Key Responsibilities Partner with leadership to develop and execute research strategies. Design and conduct MACS, collaborative studies, and IIRs in compliance with all applicable guidelines. Manage project prioritization, resource needs, operational planning, and reporting. Represent US Medical in external...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the Role As a member of Takeda Oncology, your work will contribute to our bold, inspiring vision: We aspire to cure cancer. Here, you'll build a career grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Scientific Communications Group Lead, Solid Tumors. As a subject matter expert on scientific publications best practices and the development of scientific communications strategy and deliverables, the Associate Director, Scientific Communications Lead, Solid Tumors proactively defines and drives the publication and scientific...

Help shape how Nurix communicates its science to health authorities and the world. As Associate Director, Regulatory & Medical Writing, you’ll independently lead the authoring, review, and approval of critical regulatory documents across our pipeline - from clinical protocols to health authority submissions. It’s a chance to bring clarity and strategic messaging to the documents that move our therapies through development and toward patients. Position Description The Opportunity Author and manage authoring of Regulatory & Medical Writing documents together with cross-functional collaborators; ensure content consistency within a document and across documents for a particular asset, including the development of strategic messaging and data presentation in accordance with Nurix standards and health authority requirements, for documents such as: Clinical study protocols and clinical protocol amendments Clinical study reports Investigator's brochures and annual updates...

Vacancy Name Associate Director, Medical Science Liaison, Oncology Gulf Coast Vacancy No VN799 Employment Type Full Time Location of role Remote US Department Medical Affairs US Key Responsibilities The Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of Immunocore. Candidates for this role should be located within the territory (KY, TN, AL, MS, AR, LA) Key Responsibilities: Develops and maintains in a self-driven manner outstanding knowledge of immuno-oncology and relevant disease areas Develops and maintains in a self-driven manner outstanding knowledge of Immunocore products, competitor products, and other therapeutic options within therapeutic area Collaborates with cross functional team to ensure the...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose: Scientific and Clinical Experts (SEs/CEs) are individuals who are noted for their expertise in a therapeutic area and as a result have special needs for in-depth and cutting-edge scientific information, because they treat patients, design and implement novel research, and educate colleagues and students. The Medical Science Liaison (MSL) program is specifically designed to meet these needs through a field-based group of medical...

Medical Account Associate Director – MM Rocky Mountain BioSpace – Denver, CO – Application closes January 16, 2026. About The Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups in the organization. From healthcare provider interactions and FDA regulatory strategy to medical education and data collection, CMR is involved in every phase of product development. Patient‑centered focus drives our mission to improve quality of life worldwide. Position Overview Within Field Medical Affairs (FMA) this role directs clinical engagement efforts and develops/implements medical account strategies for NNI products in priority Managed Markets accounts. The incumbent serves as the primary Medical Affairs point of contact for key payers, providing evidence‑based scientific information and maintaining strong relationships with executive decision makers, thought leaders, and business influencers. Lead clinical...

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life‑threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR‑T), T‑cell receptor (TCR‑T), natural killer (NK) cell‑based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting‑edge therapies for patients worldwide. Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta‑cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance...