- Merck & Co. (Rahway, NJ)
- …network and further through to distribution and management of materials to the clinical site . The incumbent must have demonstrated understanding of E2E product ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- …and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will ... Driving License:NoHazardous Material(s):N/ARequired Skills:Business, Business, Clinical Data, Clinical Databases, Clinical Site Management, … more
- Merck & Co. (Rahway, NJ)
- …10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):N/ARequired Skills: Clinical Site Management, Clinical ... programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
- Aequor (Thousand Oaks, CA)
- …efficiencies and reduce hand offs. Collaborate with cross-functional teams ( clinical operations, site management, biostatistics, stats programming, TA) ... design and implementation of both new technologies, new processes.Job Description: Clinical Trial Delivery Operating Model: Develop Data Management playbook to… more
- Formation Bio (New York, NY)
- …infrastructure for processing and analyzing large-scale medical imaging datasets from multi- site clinical trials Present imaging insights and model performance ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (NJ)
- …study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and ... with applicable policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the… more
- Merck & Co. (Chicago, IL)
- …study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and ... (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.Location: This is… more
- Taiho Oncology (FL)
- …with Taiho sponsored trials as assigned, which may include providing recommendations for site selection, clinical data presentation at site initiation or ... practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The Sr. Manager, Medical Field integrates clinical /scientific… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential 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… more
- Merck & Co. (North Wales, PA)
- …SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position, you will have the ... cross functional team.Job ResponsibilitiesResponsible for leading specific aspects of clinical /scientific execution of clinical protocol(s). This may… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- …- This position leads the scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this position, you will have the ... Job Responsibilities - Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s) . This...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ... ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience.The AVP will also be responsible… more
- Eisai, Inc (Nutley, NJ)
- …(SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets. Ensures study is ... your profile, we want to hear from you. The Clinical Trial Assistant will support all phases of ...Clinical Trial Assistant will support all phases of clinical study activities (feasibility, start-up, conduct and close-out) under… more
- Merck & Co. (North Wales, PA)
- …DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have ... management, communication, and collaboration skills in support of our clinical trials.Job Responsibilities: Responsible for the operational planning, feasibility,… more
- Merck & Co. (South San Francisco, CA)
- …of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist with a proven ... experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- …the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your ... management, communication, and collaboration skills in support of our clinical trials.Job ResponsibilitiesResponsible for the operational planning, feasibility, execution… more
Related Job Searches:
CRA Clinical Site Monitor,
Clinical,
Clinical Research Site Manager,
Clinical Site Development,
Clinical Site Director Venice,
Clinical Site Lead,
Clinical Site Manager,
Clinical Site Start Associate,
Senior Manager Clinical Site,
Site