14 associate director r d program management jobs found

Taysha GTx is seeking an Associate Director, Program Management R&D to enable planning and execution of clinical and medical affairs activities within the R&D organization. You will partner with Medical Affairs to plan and track milestones, manage risks, and ensure alignment with corporate objectives. The role requires 8–10 years in pharma/biotech project management, excellent communication, and the ability to lead cross-functional teams in a dynamic, startup-like environment. Remote in the U.S. #J-18808-Ljbffr

Taysha GTx is seeking an Associate Director, Program Management R&D to enable planning and execution of clinical and medical affairs activities within the R&D organization. You will partner with Medical Affairs to plan and track milestones, manage risks, and ensure alignment with corporate objectives. The role requires 8–10 years in pharma/biotech project management, excellent communication, and the ability to lead cross-functional teams in a dynamic, startup-like environment. Remote in the U.S. #J-18808-Ljbffr

Taysha GTx is seeking an Associate Director, Program Management R&D to enable planning and execution of clinical and medical affairs activities within the R&D organization. You will partner with Medical Affairs to plan and track milestones, manage risks, and ensure alignment with corporate objectives. The role requires 8–10 years in pharma/biotech project management, excellent communication, and the ability to lead cross-functional teams in a dynamic, startup-like environment. Remote in the U.S. #J-18808-Ljbffr

Overview of Position The Associate Director (Assoc. Dir.), Program Management R&D is responsible for providing program management support within the R&D organization driving and enabling successful execution of R&D activities for asset development. This role sits within the Taysha Program Management Office and will partner with the Medical Affairs organization, a function within R&D that works closely with various other areas of Taysha, to support strategic planning and decision making as well as tactical activity planning and tracking to ensure deliverables are aligned with strategic imperatives, thoroughly planned, and executed in a timely manner. As Assoc. Dir., working on a program with increasing complexity is anticipated which will require partnerships with external team members, as well as leads from other Taysha functions (e.g. Commercial, Patient Advocacy, R&D functions, etc.) to meet high-level clinical and corporate program milestones. While this...

Overview of Position The Associate Director (Assoc. Dir.), Program Management R&D is responsible for providing program management support within the R&D organization driving and enabling successful execution of R&D activities for asset development. This role sits within the Taysha Program Management Office and will partner with the Medical Affairs organization, a function within R&D that works closely with various other areas of Taysha, to support strategic planning and decision making as well as tactical activity planning and tracking to ensure deliverables are aligned with strategic imperatives, thoroughly planned, and executed in a timely manner. As Assoc. Dir., working on a program with increasing complexity is anticipated which will require partnerships with external team members, as well as leads from other Taysha functions (e.g. Commercial, Patient Advocacy, R&D functions, etc.) to meet high-level clinical and corporate program milestones. While this...

Associate Director, Program Management R&DThe Associate Director (Assoc. Dir.), Program Management R&D is responsible for providing program management support within the R&D organization driving and enabling successful execution of R&D activities for asset development. This role sits within the Taysha Program Management Office and will partner with the Medical Affairs organization, a function within R&D that works closely with various other areas of Taysha, to support strategic planning and decision making as well as tactical activity planning and tracking to ensure deliverables are aligned with strategic imperatives, thoroughly planned, and executed in a timely manner. As Assoc. Dir., working on a program with increasing complexity is anticipated which will require partnerships with external team members, as well as leads from other Taysha functions (e.g. Commercial, Patient Advocacy, R&D functions, etc.) to meet high-level clinical and corporate program...

Reference number: R2873020 Position Title: Field Medical Associate Director Oncology Department: Medical Specialty Care Canada Location: Remote (Field position) About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system –and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. About the Job Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. The purpose of the Field Medical Associate Director Oncology position is to develop the strategy and tactical plan for engagement with the scientific community and to oversee the...

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. The US Medical Learning Team plays a critical role in ensuring that healthcare providers are educated on the appropriate use of our medicines and have the information they need to improve outcomes for their patients. We develop learning strategies, scientific learning solutions and skill-based training to elevate the capability of US Field Medical (FM) teams to compliantly engage in high-quality scientific exchange with the healthcare...

Make an enterprise-wide impact on patient lives by driving advanced, data-driven execution and analytics strategy. AstraZeneca’s aspiration is to deliver life-changing medicines to patients in need, in pursuit of eliminating cancer as a leading cause of death! The US Medical Affairs (USMA) organization operates at the critical intersection of R&D, clinical development, and healthcare delivery, equipping healthcare providers and internal teams with actionable insights, evidence, and support amidst a rapidly evolving treatment landscape. As Associate Director, Advanced Medical Analytics, you will serve as a key technical and project leader within the Advanced Analytics and Clinical Trial Efficiency team. In this role, you will contribute to the vision, design, and deployment strategy for advanced analytics, AI/ML, and Real-World Data (RWD) solutions. You will work closely with collaborators across US Medical, R&D, and Global teams. Your goal is to speed up clinical trial...

Location: Cambridge, Massachusetts, United StatesSalary: $167,000 - $286,000Company: Wave Life SciencesPosted: Associate Director/Director, Platform and Pipeline Medical Affairs Lead Cambridge, MA, United States Job Description Wave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines to transform human health. Our RNA medicines platform, PRISM, combines multiple modalities, chemistry innovation and deep insights in human genetics to deliver scientific breakthroughs that treat both rare and prevalent disorders. Our toolkit of RNA-targeting modalities including RNAi silencing and RNA editing provides us with unmatched capabilities for designing and sustainably delivering candidates that optimally address disease biology. Our diversified pipeline is focused on our obesity, alpha-1 antitrypsin deficiency and PNPLA3 I148M liver disease programs and includes clinical programs for Duchenne muscular dystrophy and Huntington’s disease, as well...

Job Summary The Coder's primary job function is to certify accurate billing for professional services and hospital procedures. This is accomplished through review of clinical encounters, confirming correct use of diagnosis and procedural codes and application of appropriate modifiers and CCI edits. The Coder provides education to providers to ensure proper completion of the medical record. Job Specific Competencies 1. Reviews clinical encounters presented via electronic lists to ensure proper submission of services prior to billing. a. Edits and corrects diagnosis and procedural codes and applies modifiers and CCI edits as required according to coding guidelines and department policy. b. Effectively utilizes coding software and/or books to confirm coding accuracy. c. Verifies referring provider, rendering provider, department and other critical data elements are accurate prior to submission of completed coding. 2. Receives and reviews paper fee slips for hospital...

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely‑used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly‑motivated individuals who want to work in a fast‑paced environment and make a difference. If this is your profile, we want to hear from you. The Associate Director, Digital Medical Strategy is responsible for the execution and operationalization of digital initiatives that enable Medical Affairs, leveraging digital tools and platforms, AI, and integrated data and analytics. The role applies strong scientific and Medical Affairs strategic expertise to inform, evaluate,...

DescriptionWho We Are BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing...

Title: Associate Director Medical Writer Location: REMOTE Duration: 24+ months (Possibility of extension) Schedule: Initially, only ~15-25 hours per week are utilized for onboarding and training. If performance is strong, this position could be full time. Responsibilities The primary responsibilities of an Associate Director Medical Writer include, but are not limited to, leading key medical writing projects and activities across therapeutic areas and preparing (under minimal supervision) scientific and regulatory documents related to the clinical development of investigational and marketed drugs and biologics. These types of scientific and regulatory documents can include clinical study reports (CSRs), subject narratives, clinical investigator brochures, protocols, briefing documents, and sections of Investigational New Drug Applications (INDs) and New Drug Applications (NDAs)/Biologics License Applications (BLAs) (i.e., integrated summaries of safety and efficacy, product...