53 medical director oncology clinical development jobs found

GSK The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK's clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts. This role requires a physician capable of developing and executing oncology clinical trials in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents. Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex...

GSK The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK's clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts. This role requires a physician capable of developing and executing oncology clinical trials in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents. Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex...

GSK The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK's clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts. This role requires a physician capable of developing and executing oncology clinical trials in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents. Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex...

UNC Health Description *This position qualifies for our UNC Medical Center Operating Room Incentive Program, which includes up to $10,000 sign-on bonus and $20,000 commitment incentive or up to $25,000 tuition loan forgiveness. In addition, this position is also eligible for up to $10,000 in relocation assistance (based on location) and our employee referral program. Learn more about our UNC Hospitals RN Incentive Program here: https://jobs.unchealthcare.org/pages/unc-hospitals-operating-room-pacu-incentive-program Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve. The schedule for this position will be Monday through Friday, 7am-7:30pm (3 12-hour shifts/week) with call and holiday requirements. UNC Chapel Hill Main Campus is a level one trauma academic facility and includes 26 operating rooms. It is a very fast-paced environment offering multiple service...

Merck Job Description Our Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Distinguished Scientist (Executive Director) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group andin the field of gastric and esophageal cancers. The Executive Director, PDT lead will manage the entire cycle of clinical development, including development strategy, study design, initiation, execution,monitoring, analysis, regulatory reporting, publication, and presentation at national and international meeting. They will provide...

Merck Job Description Our Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Distinguished Scientist (Executive Director) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group andin the field of gastric and esophageal cancers. The Executive Director, PDT lead will manage the entire cycle of clinical development, including development strategy, study design, initiation, execution,monitoring, analysis, regulatory reporting, publication, and presentation at national and international meeting. They will provide...

GSK This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Provide strategic oversight of indirect reports who provide support for activities related to SDEA/PVASCs by: Ensuring that the direct reports provide the respective team support in consistently, efficiently and reliably delivering to regulatory requirements, third party commitments (implementation, maintenance and termination of SDE/PVASC) and organizational expectations and driving quality across the team. Ensuring the teams are staffed by appropriately skilled and trained individuals so that the team can successfully meet the required performance standards Developing and sharing pharmacovigilance and technical knowledge and experience with team members, with proven ability to support and coach direct reports Identify cases of potential noncompliance with internal and external procedures and follow appropriate procedures...

GSK Job Purpose: Ensure the development of appropriate regulatory strategies and their execution for assigned Vaccines asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key Responsibilities: Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategies and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategies. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely...

GSK Job Purpose: Ensure the development of appropriate regulatory strategies and their execution for assigned Vaccines asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key Responsibilities: Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategies and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategies. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely...

GSK Company Overview: At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. Our R&D division is dedicated to discovering and delivering transformational vaccines and medicines that prevent and change the course of disease. We are leveraging cutting-edge science and technology to build a deeper understanding of patients, human biology, and disease mechanisms, transforming medical discovery. We are revolutionizing the way we conduct R&D by uniting science, technology, and talent to get ahead of disease together. Job Description: As Principle Scientist PMed Operations specialising in Scientific Operations (SciOps), you will provide operational expertise to consistently implement the operational delivery of biomarker strategies developed by Clinical Biomarker and Virology leads within clinical trials, ensuring audit readiness at all times. You will be responsible for ensuring the appropriate...

GSK Job Purpose: Ensure the development of appropriate regulatory strategies and their execution for assigned Vaccines asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key Responsibilities: Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategies and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategies. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely...

GSK Job Purpose: Ensure the development of appropriate regulatory strategies and their execution for assigned Vaccines asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key Responsibilities: Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategies and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategies. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely...

Sharp HealthCare Hours : Shift Start Time: 8 AM Shift End Time: 8 PM AWS Hours Requirement: 10/40 - 10 Hour Shift Additional Shift Information: 2 days a week 10 hour shifts Weekend Requirements: As Needed On-Call Required: No Hourly Pay Range (Minimum - Midpoint - Maximum): $94.490 - $121.920 - $149.340 The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant's years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. What You Will Do The Medical Radiation Physicist is a position with three general functions. Under the direction of the Manager of the Radiation Oncology Department, this position will be responsible for performing...

GSK At GSK, we are committed to transforming the future of healthcare through innovation and technology. As a Product Director for Central Monitoring & Data Analytics, you will play a pivotal role in enabling industry-leading performance by applying cutting-edge solutions to deliver impactful outcomes for Clinical Operations. If you're passionate about driving innovation and solving complex business challenges, we'd love to hear from you! Role Overview: As a Product Director, you will lead the design and delivery of innovative Clinical Central Monitoring & Data Analytics products, driving forward technology strategies, product roadmaps, and user-centered solutions. You will collaborate with senior stakeholders, manage cross-functional teams (internal and 3rd party), and leverage modern technologies like AI/ML, GenAI, and Agentic AI to shape the future of GSK's Clinical Operations and Data platforms. Your leadership will be essential in delivering measurable...

GSK Job Title: Director/Senior Director, In Vivo Pharmacology - Oligonucleotide Sciences Location: 200 Cambridge Park Drive, Cambridge, MA Position Overview: GSK is seeking an experienced Director or Senior Director of In Vivo Pharmacology to join our Oligonucleotide Sciences research team. This leadership role offers an exciting opportunity to drive the design and execution of in vivo strategies for multiple discovery and platform projects. The successful candidate will report to the Head of Oligonucleotide Sciences, interface across the organization, and may have the opportunity to build and lead a small team. Key Responsibilities: Act as the single point of accountability for the design and execution of in vivo pharmacology strategies for all discovery and platform capability projects within the Oligonucleotide Sciences team. Interface with cross-functional teams, including in vitro biology, chemistry, informatics, biostatistics, disease biology, DMPK and...

GSK The Director in Epidemiology will support epidemiological strategy for programs led by the Epidemiology Cluster Head- Bacterial vaccines. The goal is to ensure high quality and on-time delivery of epidemiology data that will allow and support world-wide registration in compliance with the epidemiology plan, applicable good practices, and non-interventional studies standard operating procedures (SOP). As a Director in Epidemiology, you will provide scientific leadership in the application of epidemiological expertise and methods to answer key challenges identified across all phases of vaccine development for an asset or disease area to deliver new vaccines more efficiently and effectively to patients. This position functions within the Epidemiology Department, the organization of the Chief Medical Officer, GSK R&D; which contributes to the successful development of new vaccines. Our staff in Epidemiology provide leadership and expertise to develop and execute the...

GSK The Director in Epidemiology will support epidemiological strategy for programs led by the Epidemiology Cluster Head- Bacterial vaccines. The goal is to ensure high quality and on-time delivery of epidemiology data that will allow and support world-wide registration in compliance with the epidemiology plan, applicable good practices, and non-interventional studies standard operating procedures (SOP). As a Director in Epidemiology, you will provide scientific leadership in the application of epidemiological expertise and methods to answer key challenges identified across all phases of vaccine development for an asset or disease area to deliver new vaccines more efficiently and effectively to patients. This position functions within the Epidemiology Department, the organization of the Chief Medical Officer, GSK R&D; which contributes to the successful development of new vaccines. Our staff in Epidemiology provide leadership and expertise to develop and execute the...

Legend Biotech USA Legend Biotech is seeking an Expert Clinical Research Scientist as part of the Clinical Development team based in Somerset, NJ. Role Overview The Clinical Research Scientist (CS) in Clinical Development is an important role in the company supporting the development and life cycle of drug development projects. The Clinical Research Scientist will work closely with the Clinical Trial Lead/Medical Lead and Clinical Operations Lead to design and implement clinical trial protocols and manage sites, CROs and other associated work. In addition, the CS will support their manager to ensure program consistency & alignment across studies, working closely with cross-functional teams for achieving project goals, within timelines & with high quality. At the expert clinical research scientist level, the scientist will be expected to perform with less oversight and with higher impact across the assigned program and the organization as compared to the...

Legend Biotech USA Legend Biotech is seeking a Medical Director as part of the Clinical Development team based in Somerset, NJ. Role Overview The Clinical Research Physician (CRP) is a critical role in the company with significant impact on the development and life cycle of drug development projects. The Clinical Research Physician will provide strategic leadership to develop Clinical Development Plan (CDP), working closely with partners in Pre-Clinical, Regulatory, Safety, Medical Affairs, Translational Development, Market Access, Stats, & Project Management. Core responsibilities will encompass developing & implementing the Clinical Development Plan and providing leadership to new product development from IND to submission and managing the Clinical Research Scientists, if applicable. In addition, the position will ensure program consistency & alignment across studies, working closely with cross functional teams for achieving project goals, within...

Legend Biotech USA Legend Biotech is seeking Sr. Director Biostatistics and Data Analytics as part of the Clinical Development team based Remotely. Role Overview Legend Biotech is seeking a dynamic and strategic Senior Director of Biostatistics & Data Analytics to lead and build out the Data Analytics function across our BCMA and broader pipeline programs. This highly visible role will be responsible for overseeing all Biostatistics, Statistical Programming, and Data Management activities, ensuring the highest standards of scientific and operational excellence for our CAR-T cell therapy studies in for early and late-stage development. The ideal candidate brings deep biostatistics expertise, proven leadership, and hands-on experience in guiding clinical trial design and execution. Reporting directly to the Chief Medical Officer, this individual will play a key role in shaping Legend's data strategy, leading complex development programs, and driving...