Global Clinical Drug Supply Lead
Genmab
Genmab is seeking a Clinical Drug Supply Manager to join our Global Clinical Drug Supply Execution team in Princeton. This role involves leading the planning and execution of clinical trial supplies, ensuring compliance with GxP guidelines, and collaborating with internal stakeholders. The ideal candidate will have a bachelor's degree and over 3 years of experience in clinical drug supply or trial management. The position offers a competitive salary, robust benefits including health insurance, and a hybrid work model. #J-18808-Ljbffr
$249.97k - $388.13k
...profile of Otsuka products Leads the development and execution... ...Provides strategic leadership of the Global Medical review function and... ...of Otsuka products (both drugs and devices) through monitoring... ...Performs review and approval of the clinical trial medical coding....SuggestedContract workTemporary workLocal areaFlexible hours$299.6k
...The Vice President, Global Regulatory Affairs Strategy is a key leadership... ...scale. Key Responsibilities Lead delivery of regulatory... ...therapeutic areas (biologics, antibody‑drug conjugates, bispecifics, or... ...through late‑stage clinical, registration, launch, and post...SuggestedWork at office$286.31k - $346.95k
...working-with-us . Position Summary Global Program Leads at BMS are strategic-thinking, problem-... ...oriented business leaders who bring drug development and commercialization insights... ...Advisory Committees in the design of clinical trials and endpoints. Leads team to...SuggestedHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$341.36k - $413.65k
...Vp, Global Program Lead - Cell Therapy Working with Us Challenging. Meaningful. Life-changing.... ...strategy from candidate nomination through drug development to successful launch and... ...Leads team to develop program strategy and clinical program, commercialization strategy...SuggestedFull timeTemporary workFlexible hours$258.68k - $313.46k
...Senior Director, Global Regulatory Strategy, Neuroscience This... ...regulatory staff as global regulatory lead and US regional regulatory... ...diseases or neuropsychiatry drug development strongly preferred... ...CMC/Pharmtox/Biopharmaceutics/Clinical/Promotional. ~ Inter-dependent...SuggestedHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$238.89k - $289.48k
...lives. Read more: careers.bms.com/working-with-us .Position SummaryThe Director, Global Trial Lead (GTL) is accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$254.53k - $308.43k
...scientifically deployable for the MEG, MAP & RWE and Global Medical teams. Specifically, the role... ...Partners including WWTA, HEOR, Clinical Development, Market Access and Commercial... .... Responsibilities Build & Lead the RWD Innovation Center Establish...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$341.36k - $413.65k
...Bristol-Myers Squibb in Princeton, NJ, is seeking a Vice President, Global Program Lead for innovative lymphoma treatments. The role encompasses leading cross-functional teams and managing drug development strategies from nomination through commercialization. Ideal candidates...- ...A leading management consulting firm in Princeton, NJ is seeking an experienced Manager for its Supply Chain & Manufacturing team. This role focuses on Chemistry, Manufacturing, and Controls (CMC) while driving innovation and managing client engagements. Ideal candidates...
$340.87k - $413.05k
...Read more: careers.bms.com/working-with-us . The Asset Lead/Clinical Development Team Leader sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$94.3k - $129.95k
...Integra LifeSciences Corporation is seeking an Associate HR Program Manager in Princeton, NJ. This role focuses on leading global HR initiatives to drive operational excellence and enhance employee engagement. The ideal candidate must have a Bachelor's degree and a minimum...Remote work- ...PharmaACE is a growing Global Healthcare Consulting Firm headquartered... ...intelligence to accelerate drug development, optimize commercial... ...role. If you're ready to lead a groundbreaking new practice... ...AI, from R&D acceleration and clinical trial optimization to commercial...Worldwide
- ...personal care and cosmetic products. Ideal candidates will have 5-7 years of experience in Regulatory Affairs, strong knowledge of global regulations, and excellent communication skills. This position offers the exciting opportunity to work with cross-functional teams...Part time
- ...A leading pharmaceutical company in Princeton, NJ is seeking a Regulatory Affairs expert to drive the labeling strategy and ensure global compliance. The role involves leading cross-functional teams, mentoring peers, and executing strategic labeling initiatives. Qualified...Worldwide
$94.3k - $129.95k
...Integra-Lifesciences is seeking an Associate HR Program Manager in Princeton, NJ to lead global HR initiatives focused on operational excellence and employee engagement. Candidates should possess a bachelor's degree and at least 5 years of experience in HR project management...$170k - $190k
...Ascendis Pharma A/S is seeking an Associate Director of Global Scientific Publication Planning in Princeton, NJ. This role involves overseeing the development and execution of scientific publications, collaborating cross-functionally and managing publication strategies...Remote work- ...Bristol-Myers Squibb is seeking an Associate Director for Global Real Estate in Princeton, New Jersey. The role involves leading global portfolio strategy, optimizing transactions, and managing lease agreements. Candidates should have a bachelor's degree and at least...
- ...Bristol-Myers Squibb is seeking an Associate Director of Global Real Estate in Princeton, NJ. This role leads the strategy and transactions for the real estate lifecycle across various business sectors. The ideal candidate will have 7+ years of experience in corporate...
- ...A leading pharmaceutical company is seeking a Manager of Global Quality Compliance to oversee the review of manufacturing and packaging records, ensuring compliance with FDA regulations and Good Manufacturing Practices (GMP). This role requires a strong understanding of...
$160k - $175k
...A leading global biopharmaceutical company located in Princeton, New Jersey, is seeking a Regulatory Project Manager to provide project management leadership for key regulatory submissions. The role requires a minimum of 8 years in Regulatory Affairs with strong organizational...$160k - $175k
...A global biopharmaceutical company in Princeton, New Jersey is seeking a Regulatory Project Manager to lead key regulatory submissions. The ideal candidate will have at least 8 years of experience in regulatory affairs, a degree in life science, and strong project management...- ...are dedicated to helping people lead longer and healthier lives. We... ...and provide inputs to Supply Chain for demand planning to drive... ...to The Office of Prescription Drug Promotion (OPDP) You will build... ...the Hospital, IDN, Specialty Clinic and Group Purchasing...Contract workWork experience placement
- ...INTEGRA LIFESCIENCES CORP is seeking an Associate HR Program Manager based in Princeton, NJ, to lead global HR initiatives and manage complex projects. The role emphasizes operational excellence, employee engagement, and effective communication across regions. The ideal...Remote work
$273.92k - $410.88k
...strive to create, champion and maintain a global workplace where individuals’ unique... ...dedicated Vice President to oversee pivotal Clinical Development program in oncology. The Vice... ...including bispecific T‑cell engagers, antibody‑drug conjugates, next‑generation immune...For contractorsFixed term contractWork at officeRemote work- ...A leading biotechnology company in Princeton, NJ, is looking for an experienced Vice President to oversee pivotal clinical development programs in oncology. Candidates should possess extensive experience in clinical trials, particularly in hematology and oncology, along...
$249.97k - $388.13k
...Position Summary: The Executive Director, Global Value Evidence Lead, is a strategic leader responsible for driving the global value evidence... ...benefits: Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death &...Temporary workLocal areaFlexible hours- ...Genmab A/S is seeking a Vice President, Global Regulatory Affairs Strategy in Princeton, NJ. This key leadership role focuses on managing... ...assets throughout development phases. Responsibilities include leading regulatory strategy programs, engaging with health authorities,...
- ...A global consulting firm is seeking a Manufacturing Supply Chain Technology Manager in Princeton, NJ. The role focuses on business development and project delivery... ...collaborating on new business opportunities and leading complex consulting engagements primarily in the...
$160k - $200k
...the well-being of communities globally. At ANI... ...About the Role The Clinical Account Executive will report... ...rheumatology. Experience launching a drug in a competitive space with a... ...requirements ~ Experience leading and executing territory-level...Temporary workWork at officeFlexible hoursNight shiftWeekend workAfternoon shift$109.25k - $149.5k
...standards of care. SUMMARY The Lead Auditor, Quality Compliance... ...ISO, GMP, GDP, GCP, and GLP, global policies/procedures and... ...and to the required level. * Supply, in an agreed written format,... ...validation, regulatory compliance, clinical trials, computer systems validation...Temporary workWork experience placement
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