- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic...US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) Study Planning and Execution: Provides ... Budget; Establishes effective communication between CRO / vendors / AROAdditional non- study related activities: Occasional senior management interactions at… more
- Merck & Co. (Rahway, NJ)
- …effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying… more
- Merck & Co. (Rahway, NJ)
- …of entire Clinical Teams in the execution of clinical studies .--Will report and work collaboratively with the- Associate Vice President to promote ... Job DescriptionOur Clinical Development teams manage studies to...safety and efficacy as well as new drug applications, clinical study reports, or publications.Participation in internal… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...you ready to make a difference? The Position The Associate Director, Research Partnerships (RP) is responsible for developing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … clinical activities beyond phase 3a (phase 3b workshops, Investigator Spon- sored Studies ) Evaluation and decision of clinical trial proposals from Regions & ... NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating...you ready to make a difference? The Position The Associate Global Medical Director will serve as a pivotal… more
- Aequor (Thousand Oaks, CA)
- …team members ensure supply to patient every time. During the length of the clinical trial, the study planner is responsible to monitor inventory at central ... DSC arranges and ensures the product needed for 's clinical trials is available globally. DSC serve patients around...patients to receive their dose on time. The Global Study Planning (GSP) team is responsible for forecasting &… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... a living. Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory… more
- United Therapeutics (Annapolis, MD)
- …for patients and keen eye for detail make you the perfect candidate for the role of Senior Clinical Research Associate . In this role, you will be the expert ... off-site monitoring activities, ensuring the rights and well-being of study subjects are protected, trial data is accurate, complete,...of clinical research? Join us as a Senior Clinical Research Associate -… more
- Avania (OR)
- Avania are hiring for the key role of experienced Clinical Research Associate (CRA) or Senior Clinical Research Associate (Sr CRA) As a CRA/Sr CRA ... you will be the lead for several studies running in parallel, in all associated ...site management and close out activities. + Be the study lead for several studies . + Act… more
- Danaher Corporation (Chaska, MN)
- …lives with diagnostic tools that address the world's biggest health challenges. The Senior Clinical Research Associate for Beckman Coulter Diagnostics is ... + Support the in-house biorepository by receiving, shipping, and tracking clinical study samples. + May perform other clinical project activities… more
- System One (Kansas City, MO)
- Senior Clinical Research Associate - Regional Location: Home Based, Kansas City, MO Type: Full time Start Date: ASAP Are you an experienced Clinical ... site management and support to external trial staff (Principal Investigators and Study Coordinators) from trial initiation to closeout. + Ensure collection of… more
- WuXi AppTec (Austin, TX)
- …position within the Operations team and is assigned as a study lead to manage clinical trial studies . The Senior CRA will partner with a Project Manager ... every disease can be treated." **Responsibilities** **Job Summary:** The Senior Clinical Research Associate is...teams, liaise with other functional areas to accurately coordinate clinical study activities + Coordinate clinical… more
- Kelly Services (Sunnyvale, CA)
- …Clinical Research Associate is responsible for in the execution of clinical trials in addition to supporting the study site identification, monitoring ... role, you will have the opportunity to:** Execute all activities related to a clinical study , including (but not limited to): + Clinical site selection +… more
- BeiGene (San Mateo, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... ICH-GCP guidelines, local regulations, and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical … more
- IQVIA (Overland Park, KS)
- …other required study documentation. * Act as a mentor for clinical staff including conducting co-monitoring and training visits. * Collaborate and liaise with ... Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study … more
- IQVIA (Carlsbad, CA)
- IQVIA Biotech is hiring for our Early Clinical Development team. Ideal candidates will have Phase 1 Experience across a variety of therapeutics (prefer Cell & Gene ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Committees, Medical/Patient Societies). + Responsible for optimal planning and execution of clinical studies from FIM throughout pivotal, ensuring integration of ... and planning of Clinical Trial Report. Leads clinical interpretation of study results and ensures...a base salary typically between $170,000 and $269,000 for Senior Associate Director and $250,000-$394,000 for Director… more
- ICON Clinical Research (Los Angeles, CA)
- …the future of clinical development. We are currently seeking a CRA II or Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. ... lifecycle. **What You Will Be Doing:** + Monitoring clinical trial sites to ensure adherence to study... clinical trials + Extensive experience as a Clinical Research Associate , with a strong understanding… more
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