Senior Clinical Protocol and Supply Planning Lead
Merck
Merck, a global healthcare leader, seeks a Protocol CSPM to design and oversee end-to-end clinical supplies for assigned studies. You will coordinate with clinical development, regulatory, and supply chain teams to ensure timely sourcing, manufacturing, labeling, and distribution of products to trial sites worldwide. The role requires strong project management, GMP/GCP knowledge, and expertise in ERP systems, Excel, PowerPoint, and Veeva. Hybrid work arrangement in the U.S. is available. #J-18808-Ljbffr Merck
- ...Merck's Global Clinical Supply organization seeks a Senior Specialist to manage end-to-end clinical supply chain... ...activities for assigned studies. The Protocol Clinical Supplies Project Manager designs strategic and operational plans, serves as primary contact for internal...Senior
$117k - $184.2k
Job DescriptionThe Global Clinical Supply (GCS) organization is accountable... ...GCS is accountable for the planning, sourcing, labeling,... ...Working independently, the Protocol Clinical Supplies Project Manager... ...with clinical partners and senior leaders.Responsible and accountable...SeniorFull timeFor contractorsLocal areaFlexible hours$117k - $184.2k
Job DescriptionThe Global Clinical Supply (GCS) organization is accountable... ...GCS is accountable for the planning, sourcing, labelling,... ...for clinical supply needs per protocol and ensuring a robust signal... ...with clinical partners and senior leaders.Responsible and accountable...SeniorFull timeFor contractorsLocal areaFlexible hours- Merck is seeking a seasoned Inventory Manager Clinical Supplies Project Manager to lead end-to-end planning and execution of clinical materials. You will collaborate with GCS Planning, CTT, and regional teams to ensure timely packaging, labeling, and distribution of CFGs...Senior
$117k - $184.2k
...Merck seeks a Senior Specialist to manage clinical supply chain planning and inventory for global clinical trials. The role involves coordinating end-to-end clinical supply activities, collaborating across functional teams, and ensuring timely delivery of materials to...SeniorWork at office- Merck seeks a Senior Specialist, Business Analyst, Launch Planning to lead business analysis and process design for Strategy and Planning and Launch Planning within Content Supply Chain Orchestration. The role partners with managers, product teams, and cross-functional...Senior
- ...Senior Principal Scientist position leading clinical research strategy and execution for oncology drugs across all development phases. Responsible for study design... ...healthcare organization. Responsibilities Plan and direct clinical research activities for investigational...Senior
- Johnson & Johnson's Therapeutic Area in Spring House, PA is seeking a Senior Clinical Scientist to support clinical research across early to late-phase development. You will assist with protocol development, data review, and regulatory document preparation, collaborating...Senior
$282.2k
...We are seeking a passionate and experienced Senior Principal Scientist specializing in Breast Cancer... ...worldwide.Responsibilities:Evaluate pre-clinical and translational work for generating early clinical development plans and Investigational New Drug applications.Develop...SeniorFull timeFor contractorsLocal areaWorldwideFlexible hours$282.2k
...Senior Principal Scientist position in breast cancer clinical research at a pharmaceutical company. Responsibilities include developing... ...develop early clinical development plans and IND applications Design clinical trial protocols and operational plans aligned with development...Senior- ...Senior CRA/ CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines... ...clinical trials. Ensuring protocol compliance, data integrity,... ...Retirement and pension plans Life assurance and disability...SeniorRemote work
- ...Senior Clinical Trial Manager - Remote, US ICON is a global healthcare... ...As the clinical operations lead, you will work cross-functionally... ...effective study oversight plans, monitoring strategies, and risk... ...trial activities comply with protocol requirements, ICH-GCP...SeniorRemote work
- CSL Behring is seeking a senior professional to manage global supply and inventory planning across sites/CMOs in a hybrid model. You will develop 3- to 36-month horizon plans and integrate strategic demand with operational execution, driving capacity optimization and cross...
- ...Clinical Scientist - Infectious Disease (HIV) - Home Based (US/Canada... ...What you will be doing: May lead or support a study or studies,... .../scientific execution of the protocol. As lead, will be... ...development of the Medical Monitoring Plan (MMP) and review of SAE reports...SeniorRemote workWork from homeWorldwideWork visaFlexible hours
$109k - $174.8k
...Function: Discovery & Pre-Clinical/Clinical Development... ...Job Description: Senior Clinical Scientist Clinical... ...Scientists Clinical Leads and other cross-... ...development of clinical trial protocols and study materials... ...the clinical development plan ensuring compliance with...SeniorFull timeWork at officeImmediate start$110.52k - $138.15k
Senior Clinical Research Associate At ICON Strategic Solutions, you will... ...they are conducted according to protocol, regulatory requirements, and... ...You Will Do: You will lead on clinical trial monitoring... ...applicable Retirement and pension plans Life assurance and...SeniorFull timeWorldwide- ...Merck seeks an Associate Principal Scientist to lead early-phase clinical trial design, planning, and execution within Translational Medicine. The role... ...ICH, and regulatory requirements Author clinical protocols, investigator brochures, study reports, regulatory submissions...
$190.8k - $300.3k
...to serve as an Immunology Biomarker Lead within Translational Clinical Biomarkers. This role provides strategic... ...biomarker analysis plans and provide critical scientific input... ...Personalized Medicine, Pharmacodynamics, Protocol Development, Rheumatology, Translational...Full timeFor contractorsLocal areaFlexible hours$262.06k - $306.73k
...our shared purpose: leading the fight against MASH... ...the right way. The Senior Director, Clinical Operations provides... ...operational leadership for the planning, execution, and... ...aspects of protocol development, study design... ...Safety, Quality, and Supply Chain Planning & Operations...SeniorMinimum wageFull timeLocal areaFlexible hours$190.8k - $300.3k
...Senior Principal Scientist in Regulatory Affairs at Merck responsible for developing... ...Serve as global regulatory lead and single point-of-contact for assigned... ...strategy discussions Prepare IND/CTAs, clinical study reports, protocols, and worldwide marketing applications...SeniorWorldwide- Katalyst CRO is seeking an experienced SDTM expert with deep SAS programming skills to lead data processing and macro development for clinical trials. You will collaborate with biostatisticians and study teams, review CDISC-compliant specifications, and ensure accuracy...Senior
$61k - $155k
...strong expertise in SAS and a solid understanding of CDISC standards. The ideal candidate will have 5-7 years of experience in the clinical domain. This position offers a pay range from $61,000 to $155,000 per year, plus potential performance-based bonuses and...Senior- ...Description Description The Senior Director (Sr. Principal Scientist... ...as the Global Regulatory Lead to Product Development Teams... ...of local registration study protocols when needed to obtain marketing... ...Worldwide Marketing Applications, Clinical Study Reports, protocols,...SeniorLocal areaWorldwide
$142.4k - $224.1k
...Medicine (TMed) drives early clinical development of novel... ...for the design, planning, and execution of early... ...development teams. May lead development of departmental... ...for authoring clinical protocols, investigator brochures... ...escalation and mitigation, senior management...Full timeFor contractorsLocal areaWorldwideFlexible hours$282.2k
...Senior Principal Scientist leading clinical research strategy and execution for breast cancer oncology medicines across all development phases. Responsible... ...research and develop early clinical development plans and IND applications Design and oversee conduct of clinical...Senior$190.8k - $300.3k
Job DescriptionDescriptionThe Senior Director (Sr. Principal... ...advice as the Global Regulatory Lead to Product Development Teams... ...of local registration study protocols when needed to obtain marketing... ...Worldwide Marketing Applications, Clinical Study Reports, protocols,...SeniorFull timeFor contractorsLocal areaWorldwideFlexible hours- ...Madrigal Pharmaceuticals seeks an experienced physician to lead early-phase clinical development programs and translational strategy for... ...including first-in-human and Phase 1/1b trials Lead study protocol development including patient population selection, endpoint...Senior
$72 - $82 per hour
...comprehensive benefits plan that includes the following... ...that believes in leading with our values. Feel... ...and supported with PPE supplies, comprehensive infection prevention protocol, daily pre-screens, and... ...conditions; reporting changes to Clinical or Client Services...SeniorWeekly payFull timeWork at officeLocal areaFlexible hoursWeekend work- The Opportunity:In collaboration with the Lead Counsel, Global Clinical Development, as the Associate Director, Senior Counsel, Clinical, you will provide practical, timely... ...manufacturing agreements, and clinical trial supply.Collaborate with the R&D/Strategy...SeniorFull timePrivate practiceWork at office
$282.2k
...Senior Principal Scientist position leading clinical research strategy and execution for hematology oncology medicines... ...develop early clinical development plans and Investigational New Drug... ...overseeing clinical studies and protocols Strong scientific publication...Senior
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