Global Regulatory Program Manager — Oncology (1yr)
Medasource
Medasource is seeking a Regulatory Program Manager to lead global regulatory strategies and execution for oncology programs. The role requires coordinating cross-functional teams, managing submissions, and accelerating timelines. Expect a high-visibility, hybrid work arrangement in the US. The RPM will partner with the GRL and GRT, guide planning, and mentor other RPMs while driving process improvements across programs. #J-18808-Ljbffr Medasource
$164k - $282.9k
...medicines of tomorrow. Our Oncology team is focused on the... ...for the Director, Global Medical Affairs... ...Affairs SharePoint Site Management/Scientific and Knowledge... ...marketing directors, regulatory leaders, outcomes research... ...s long-term incentive program.Subject to the terms...SuggestedFull timeLocal areaImmediate startWorldwide$193.04k - $289.56k
...are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases,... ...by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable... ..., and society.Job SummaryThe Global Regulatory Lead (GRL) is responsible for leading...Suggested- ...times onsite per week) ASAP start The Regulatory Program Manager (RPM) will be an asset-level... ...translation and distillation of overall global regulatory strategy to executable plans... ...speed in the delivery of the clients Oncology portfolio. Key Responsibilities: · Empower...SuggestedContract workImmediate startWorldwideFlexible hours
- ...cost, and time objectives are met. You will mentor Project Directors and Project Managers, collaborate with study sponsors, and optimize profitability while ensuring regulatory compliance and risk management across global programs. #J-18808-Ljbffr Precision For MedicineSuggested
$150k - $258.75k
...Johnson Innovative Medicine's Global Commercial Strategy... ...communications.Demonstrated ability to manage multiple priorities, operate... ...Therapeutic area experience in oncology, immunology, neuroscience,... ...Management, Product Strategies, Program Management, Strategic...SuggestedFull timeLocal areaImmediate start- Roche in New Jersey seeks an experienced Regulatory Affairs professional to support global medical diagnostic products. The role involves registering and addressing affiliate questions, improving processes with RPA, and ensuring regulatory compliance across US and international...
- ...Chief Medical Officer. The role oversees due diligence, licensing, and integrations, coordinating with global partners to deliver on business needs while ensuring regulatory compliance. Travel up to 10% may be required. The position requires a Bachelor’s degree with 8+...Work at office
- ...Johnson & Johnson seeks a Director, Global Medical Affairs Strategy & Execution in Raritan, NJ. You will partner with GMAL to own strategy, generate integrated evidence plans, and lead publications across designated therapeutic areas. This role requires significant...
- ...including immunology, oncology and neuroscience - and... ..., implementation, and global governance of Environmental... ..., and Safety (EHS) programs within assigned scope.... ...oversight of EHS regulatory compliance. Own the... ...incident investigation and management process. Develop...Full timeTemporary workLocal area
$117k - $201.25k
.../Clinical DevelopmentJob Sub Function: Regulatory ScienceJob Category:Scientific/TechnologyAll... ...best talent for Principal Scientist (Manager), Global Regulatory Affairs, CMC.Purpose: The... ...participate in the Company’s long-term incentive program.Subject to the terms of their...Full timeLocal areaImmediate start$116k - $200.1k
...patients on their journey to wellness. Learn more at The Global Supply Network Planning Sr. Manager is responsible for leading and developing a team of... ...in English is required. ~ Proficient in MS office programs: Word, Excel, PowerPoint, Project Planning, Flow...Full timeLocal areaImmediate startWorldwideNight shiftEarly shift- Daiichi Sankyo US in New Jersey seeks a Global Regulatory Lead to shape regulatory strategy for development programs and represent regulatory in GPT meetings. You will guide... ...US, and strong cross‑functional leadership in oncology-focused development. Travel up to 20%. #J-188...
$127.28k - $190.92k
...are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and... ...by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable... ...families, and society.Job SummaryThe Manager FP&A position is an integral part of the...$127.28k - $190.92k
...advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases... ...2030 vision to "be an innovative global healthcare company contributing to the... ..., and society.Job SummaryThe Manager, EDC Database Programming is a member of the Biostatistics and...- Johnson & Johnson is seeking a Director, Global Portfolio Strategy & New Business Development in Raritan, NJ. The role leads cross-functional... ...to drive strategic initiatives, investments, and lifecycle management to deliver sustained growth. Required are 7+ years in strategy...
$122k - $245k
...recognize their merit.Job Function: Project/Program Management GroupJob Sub Function: Technology... ...discipline of DePuy Synthes' global cybersecurity function. This leader will... ...patient trust, business continuity, and regulatory compliance. This position reports into...Full timeLocal areaImmediate startShift work$178k - $307.05k
Johnson & Johnson MedTech is hiring a Sr. Director, Regulatory Law in New Brunswick, NJ. This role involves providing expert legal counsel on U.S. and global regulatory law for DePuy Synthes. The position requires collaboration with multiple teams to support regulatory...- ...please visit We Are:Guest Worldwide is a global collective of dynamic, industry-leading... ...leadership for procurement, category management, and supplier strategy across a global,... ...Supplier Relationship Management (SRM) program, including segmentation, governance, and...Full timeLocal areaWorldwide
$271.5k
...advancing breakthrough therapies in oncology, cardiovascular disease, rare... ...vision to "be an innovative global healthcare company... ...& Strategy role oversees and manages US Medical Affairs activities... ...for lifecycle management, IIS programs and post approval clinical programs...$255k - $425k
...Planning and Operations. This role involves leading all CSO-related activities for oncology and specialty medicine drug candidates, ensuring effective management of clinical supplies globally. The ideal candidate will have a robust scientific background, extensive...$164.2k - $218.9k
...Requirements The OpportunityThe Head of L&D - Global Technology & Operations is responsible... ..., adopted, and reinforced at scale.· Manage partnerships with HR and business leaders... ...work rather than delivered as stand‑alone programs.· Coordinate enterprise and delivery partners...Full timeTemporary workWork at officeLocal areaRelocation package3 days per week- Merck & Co. is looking for a Senior Director, Clinical Safety Science, to shape and advance global safety strategy throughout the product lifecycle. This leadership role oversees a team of Safety Scientists, ensuring proactive safety surveillance and risk mitigation. The...
$242.7k - $404.5k
Daiichi Sankyo US is looking for a Senior Director, Clinical Safety Science to lead global safety strategy across the product lifecycle. This key role oversees a team of Safety Scientists and collaborates with various stakeholders for proactive safety surveillance and...- A leading tech firm is seeking a Product Manager with extensive experience in regulatory submission processes and health authority queries. The role requires... ..., especially those familiar with TransPerfect Global Link Enterprise. This position offers the chance to support...
$162.4k - $243.6k
...are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases,... ...our 2030 vision to "be an innovative global healthcare company contributing to the... ...SummaryThe Associate Director, US OBD Program Management provides strategic, operational, and financial...Work at office$171.12k - $256.68k
...are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases,... ...by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable... ...of this job is to provide statistical programming technical support related to R...- ...registries) including data management activities in... ...years’ experience in Oncology is mandatory.• CTOM needs... ...rapidly gain knowledge with programming/query languages•... ...Clinical Supplies Platform, Regulatory, Pharmacokinetics and... ...action plan at global CSU/sites level if needed...Immediate startFlexible hours
- ...portfolio strategy, governance, and performance management. You will partner with senior leaders to drive cross-functional programs and ensure value realization across the CSPV... ...to improve efficiency and outcomes across global initiatives. #J-18808-Ljbffr Daiichi Sankyo...
$137.6k - $180k
...endocrinology, metabolic, hematology and oncology franchises. RRD is dedicated... ...Reports To: Director, Regulatory Affairs - Advertising,... ...Direct Report(s): None Areas Managed: Advertising & Promotion North... ...of product messages, assets, programs, tactics, etc. •...Full timeTemporary workNight shiftWeekend work$102k - $177.1k
...America, Texas (Any City)Job Description:The Manager Deliver Operations Planning is... ...ResponsibilitiesDeliver Operations Planning ExecutionLead global execution of Deliver Operations Planning... ...Deliver/Strategy and management of large programs.Proven success working in a complex,...Full timeLocal areaImmediate start
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