Associate Director, Global Clinical Supply Chain
Orro
Orro is seeking a Supply Chain Manager in Cambridge, MA to oversee the strategic and operational management of clinical supply activities. This role requires expertise in supply chain strategy and vendor oversight while ensuring compliance with regulations. The ideal candidate will have extensive experience in global supply chain for clinical trials, with excellent communication skills and the ability to work in a dynamic environment. Flexible travel is expected as part of the role. #J-18808-Ljbffr Orro
- ...strategic and operational management of clinical supply across all development phases. You will... ...delivery of investigational products to global sites and partner with Clinical Operations... ...years in pharmaceutical/biotech supply chain, with deep experience in global clinical...Suggested
$154.4k - $242.55k
...DescriptionOBJECTIVES/PURPOSE: • The Associate Director, GCSC Operations Lead is... ...of GCSC activities globally. Under the direction of the... ...Associate Director manages Clinical Supply project delivery in support... ...leads Global Clinical Supply Chain group initiatives including...SuggestedMinimum wageContract workTemporary workLocal areaRemote work- ...operational management of complex clinical supply activities across all phases... ...deep expertise in supply chain strategy and vendor... ...with a strong understanding of global GMP and regulatory requirements... ...& Regulatory on activities associated with labelling, packaging, specifications...SuggestedFlexible hours
$273.21k - $331.06k
...Associate Director, Global Clinical Physician, Neuroscience Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work...SuggestedHourly payFull timeTemporary workPart timeFor contractorsSummer workWork at officeRemote workWorldwideFlexible hours$183k - $252k
About the RoleThe Global Associate Medical Director, Evidence Generation and Education is a key member of the Global Medical Rare Disease team, reporting... ...of Global Medical SMA and ALS teams by translating clinical, real-world, registry, and emerging scientific data into...SuggestedFull timeTemporary workLocal areaWorldwide- ...strategic and operational management of complex clinical supply activities across all phases of... ...Develop and implement end to end supply chain strategies from raw material to finished... ...external vendors in compliance with GMP and global regulations Develop Interactive...
- ...into Phase 1 and Phase 2 clinical studies to enable proof of... ...need. Position Summary The Associate Director, Clinical Supply will lead clinical supply... ...activities, shipment planning, and global distribution of... ...assessing potential supply chain constraints, manufacturing...
$200k - $240k
Associate Director, Clinical Supply Chain At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically... ...hands‑on clinical supply planning and execution across global Phase 1 and Phase 2 studies. This role owns clinical...Local area$150k - $200k
...operational management of complex clinical supply activities across all phases... ...deep expertise in supply chain strategy and vendor... ...with a strong understanding of global GMP and regulatory requirements... ...& Regulatory on activities associated with labelling, packaging, specifications...Flexible hours$185k - $200k
...demands Solid experience developing clinical labels Experience developing IRT... ...presentations here. About the Role Associate Director, Clinical Supply Chain As the Associate Director of... ...management Develop and implement global Clinical Supply Chain strategies Manage...Work at officeFlexible hours$142.5k - $256.5k
The RoleAssociate Director, Clinical Supplies Project Management is responsible for... ...manage programs and their associated clinical studies. Provides... ...degree preferred)Prior Cold Chain distribution experience requiredIRT... ...’s why our US benefits and global well-being resources are...Permanent employmentFull timeWork from home- Job DescriptionThe Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data, design of clinical trials, identification and investigation of safety signals, management...Worldwide
$194k - $267k
About This Role As the Associate Medical Director, Global Drug Safety, you will play a pivotal role in safeguarding patient well-being and shaping... ...scientific leader within Global Pharmacovigilance, applying your clinical expertise and sound judgment to ensure the highest...Full timeTemporary workLocal area$170k - $182k
The Associate Director position within Clinical Supply Chain provides strategic leadership and oversight for end-to-end supply chain management across multiple... ...to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland...Work at officeLocal areaFlexible hours3 days per week- Biogen is seeking a Global Associate Medical Director to lead evidence generation and education for SMA and ALS across the Rare Disease portfolio.... ...compliance with GCP and internal policies while collaborating across Clinical Development, Biostatistics, #J-18808-Ljbffr Biogen
$166.79k - $218.92k
Introduction to Role Are you ready to make a difference in the lives of patients with rare diseases? As an Associate Global Medical Director, you will report to the Senior Director and play a crucial role in planning, tactical execution, and leadership for haematology,...Hourly payTemporary workWork at officeLocal area$198.5k - $311.85k
...empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area... ...through life-changing work. Certified as a Global Top Employer, we offer stimulating... ...leads and drives strategy for clinical studies within the overall global clinical...Minimum wageTemporary workWork at officeLocal areaRemote workNight shift- A leading healthcare solutions provider is seeking an Associate Director, Clinical Program Quality Leader in Cambridge, MA. The candidate will provide quality assurance oversight for clinical research programs, ensuring inspection readiness and GCP compliance. A minimum...Hourly pay
- Aditum Bio in Cambridge, MA seeks Associate Director, Clinical Supply to lead end-to-end clinical supply planning, forecasting, packaging, labeling, distribution, and inventory management across its portfolio. This role reports to the SVP of CMC and collaborates with portfolio...
- ...Cambridge, Massachusetts, is seeking a highly skilled individual to lead strategic management of clinical supply activities. The role requires a strong background in supply chain strategy and vendor oversight, along with excellent communication skills to work in a fast-...
$170k - $210k
...are passionate about delivering the possible to patients, and who lead with the desire to work on novel ideas.As an Associate Director, Clinical Supply Chain Lead, you will report to the Senior Director, Supply Strategy & S&OP to assume accountability for end-to-end...Temporary workImmediate startFlexible hours$175k - $226k
...About eGenesis eGenesis is a clinical-stage biotechnology company developing human-compatible... ...organs to address the severe global organ shortage. The Company’s proprietary... ...is headquartered in Cambridge, MA. The Associate Director, Clinical Science is responsible for the...$176.1k - $287.3k
...across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the... ...fit-for-purpose assays that meet global regulatory requirements and support clinical... ..., manufacturing readiness, and supply planning with IVD partners to ensure...$163.2k - $244.8k
Job DescriptionGeneral Summary:The Associate Director, Global Submission Management (GSM) is responsible for the strategic oversight and execution... ...management, regulatory operations, or regulatory/clinical project managementExperience managing routine, regional, and...Full timeSummer workRemote workFlexible hours2 days per week$174k - $196k
...Associate Director, Clinical Pharmacology Cambridge, Massachusetts, United States Associate Director, Clinical Pharmacology City Therapeutics... .... ~ Prior participation in FDA, EMA, or other global regulatory agency interactions. ~ Familiar with translational...Work at officeWork from homeFlexible hours$146.3k - $234.1k
...medicine through cutting-edge science and innovation. As Associate Director, Clinical Pharmacology & Pharmacometrics, you will play a pivotal role... ...books, NDA/BLA submissions) Represent BioNTech at global health authority meetings, providing clinical pharmacology...Hourly payWorldwide$176.1k - $287.3k
...Associate Director, Clinical Diagnostics (CDx) This role provides an exciting opportunity to lead projects... ...fit-for-purpose assays that meet global regulatory requirements and support... ...transfer, manufacturing readiness, and supply planning with IVD partners to ensure...- ...Associate Director/ Director, Clinical Pharmacology | Commercial Biotech Full Relocation Support Offered (if relocating from outside MA) APX Life Sciences... ...analyses. Prepare Clinical Pharmacology components for global regulatory submissions and support health authority...RelocationRelocation package3 days per week
$148k - $236.5k
.... Position Summary:Pioneering Medicines is seeking an Associate Director or Director, Clinical Development Operations to join our growing team and take... ...working knowledge of ICH-GCP, FDA, EMA, and other global regulatory requirements.Proven success managing multi-site...For contractors$160k - $240k
Who we are:Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines... ...:Contribute to the planning, implementation, and execution of global clinical trials.Plan, execute, and lead study-specific meetings...Contract work
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