7 associate director ethics compliance jobs found in Cambridge

Biogen Biogen's Decision & Quality Analytics Innovation (DQAI) team is part of Portfolio Leadership, Analytics & Insights (PLAI), which is under the Development department. The vision of the DQAI team is to deliver trusted insights that drive smarter decisions and measurable impact across the research, development and medical (RDM). We are seeking an experienced and highly motivated Associate Director of Data Management & Stewardship to join our team. This individual will take ownership of managing all aspects of our team's data - from acquisition and stewardship to governance and cross-functional alignment. The role will ensure that our data foundation is robust, well-governed, and positioned to enable advanced analytics, including AI/ML, simulation, etc. and ultimately support critical portfolio decision-making. Key Responsibilities Develop process of overseeing the full lifecycle of PLAI data across research, development, and quality functions is...

Biogen About This Role The Associate Medical Director, Scientific & Value Communications role is a part of the US Medical Team, acting as a strategic partner that helps inform medical practice across Multiple Sclerosis and Neuropsychiatry therapeutic areas to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Scientific Communication Plan, the Associate Medical Director, Scientific & Value Communications will ensure consistent, compliant and impactful communications via publications, congress activities and medical education. This individual contributor role supports Multiple Sclerosis and Neuropsychiatry US marketed products and reports to the Head of Scientific & Value Communications, US Medical. What You'll Do Contribute to the development of successful and compliant execution of the Scientific & Value Communications strategy, including publications (abstracts, posters, manuscripts),...

Biogen About This Role The Associate Medical Director, Evidence Generation role for rare disease is a part of the US Medical Team, a strategic partner within Biogen, that helps inform medical practice in our rare disease medical team and pipeline to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Evidence Generation plan, the Associate Medical Director, Evidence Generation will lead the implementation of a cross-portfolio evidence generation plan and successfully deliver the plan using a balance between technical expertise, therapeutic knowledge, project and communication skills, leveraging and prioritizing internal and external resources as required. This individual contributor role supports the full portfolio of US marketed and pipeline products and reports to the Head of Evidence Generation. What You'll Do Coordinate or lead the development of quality, impactful evidence generation activities,...

Biogen About This Role As Associate Director, Regulatory CMC Small Molecule Lead, you will play a pivotal role in shaping and executing the global Regulatory Chemistry, Manufacturing and Controls (RegCMC) strategy for Biogen's small molecule portfolio. You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delivery of high-quality regulatory submissions that support product development, registration, and lifecycle management. This position requires a strategic thinker and strong communicator with deep regulatory CMC expertise who thrives in a global, matrixed environment. What You'll Do The Associate Director, RegCMC Small Molecule Lead oversees the management and coordination of regulatory CMC activities across assigned projects and products. Primary duties include: Lead cross-functional teams responsible for global RegCMC submissions (IND/IMPD/CTAs, NDAs/MAAs) and responses to Health Authority...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. Title: Associate Director, US Regulatory Advertising & Promotional Labeling The Company: With deep expertise in chemistry, Nuvalent is creating selective medicines to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the VP, US Regulatory Advertising & Promotional Labeling, the Associate Director US Regulatory Advertising & Promotional Labeling will...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Senior Director, Payer & Reimbursement, the Associate Director, Pricing & Contracting Operations plays a critical role in shaping and executing the company's pricing and contracting strategies to optimize access to Nuvalent's product portfolio, as well as playing a key part in driving pricing and contracting strategy and management. We are a growing pharmaceutical company with a commitment to delivering innovative, oral targeted therapies for oncology patients. We are seeking a dynamic and strategic professional to lead pricing and contracting operations....

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Associate Director, Scientific Communications, the Senior Manager, Medical Information will be responsible for ensuring the quality and medical accuracy of promotional and non-promotional materials. This individual will represent Medical Affairs in a cross-functional review committee, working closely with Medical, Regulatory, and Legal functions, and ensure the scientific balance, medical accuracy, and scientific validity of materials. This role will also support the development, maintenance, and dissemination of standard and custom Medical Information response...