- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThis position drives scientific planning, strategy and execution of Phase 1-4 clinical studies .-Under the direction of the Program Lead, you will ... collaborate with global, cross- functional team-members including clinical directors and study managers to... deliverables.Participates in the set up and design during study start up (eg, database set up)Lead… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …North America Clinical Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...and accountable for tasks, processes and deliverables from trial start up through closure, including but not limited to:… more
- Insmed Incorporated (Bridgewater, NJ)
- …operational support for the Clinical Operations team with heavy focus on study start ‐up activities, patient recruitment efforts, maintenance, and study ... Operations objectives by providing operational support to the clinical study team (CST) with the responsibility...understanding of the DIA TMF Reference Strong familiarity with study start ‐up activities, including feasibility, country and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …opportunity employer including veterans and people with disabilities. Summary The Associate Director, External Data Management, is accountable for the end-to-end ... delivery of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).ResponsibilitiesReconcile the TMF document trackers… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …has expanded our academic prowess and the potential to conduct innovative clinical trials to impact respiratory diseases. While NYMC's primary mission is training ... research on the prevention, treatment, and cure of respiratory disease. LBRI studies respiratory health issues of concern to scientists and health care experts… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …Lovelace Biomedical and its Commercial Clients throughout the prospecting, award, and study closure stages. The position will be responsible for overseeing the life ... cycle of a scientific program with the Scientific Operations staff from start to finish driven by a clear understanding of both Client and CRO needs and… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …can be based in Armonk, NY, Basking Ridge, NJ or Uxbridge, England._ The Assoc Mgr Clinical Study (CSAM) role supports the Clinical Study Lead (CSL) ... of CROs deliverables will vary accordingly. The Assoc Mgr Clinical Study works with the study... sites may be required to assist with monitoring clinical studies . **A typical day as a… more
- ICON Clinical Research (Wilmington, NC)
- …the friendliest people in the sector, and you'll be helping shape an industry. As a ** Study Start -Up Associate Intern,** you will play a vital role in the ... internship opportunity provides valuable hands-on experience in the crucial study start -up phase of clinical ...play an integral role in the successful initiation of clinical studies . Your contributions will directly impact… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP). **Responsibilities** - Reconcile the TMF… more
- ThermoFisher Scientific (Memphis, TN)
- **Job Description** **Distribution Study Associate ** When you are part of the team at Thermo Fisher Scientific, you will do important work, like helping ... **How will you make an impact?** As a Distribution Study Associate , you will be responsible for...+ Responsible for timely order entry and delivery of clinical study materials and clinical … more
- Fenway Health (Boston, MA)
- …the direction of The Fenway Institute's Associate Medical Director and the Clinical Research Operations Manager, the Study Coordinator will work with staff ... The Fenway Institute, and other involved parties + Leads study start -up and site monitoring visits for...and trainings + Develops and implements recruitment plans for studies . + Meets regularly with study staff… more
- Abbott (Alameda, CA)
- …. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality ... levels with our new sensing technology. **The Opportunity** The Associate Clinical Research III will assist in...and track resolution of action items. + Participate in study start up activities. + Responsible for… more
- Stanford University (Stanford, CA)
- …Research Coordinator Associate to perform duties related to the coordination of clinical studies . Coordinate moderately complex aspects of one or more ... Clinical Research Coordinator Associate : Fixed Term - 1 Year **School...clinical studies . Work under close direction of the two principal investigators… more
- Abbott (Alameda, CA)
- …. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality ... Responsible for the design, execution and monitoring of internal clinical studies . + Participate in the design,...and track resolution of action items. + Participate in study start up activities. + Responsible for… more
- Hartford HealthCare (Hartford, CT)
- …efforts to initiate new studies , attending IRB meetings to expedite the start -up process. The CRA supervises all study activity and may delegate ... analysis and development of protocols. * Enrolls patients in studies by screening for eligibility criteria, consulting with physicians...of study activity as required of a Clinical Research Associate * * Bachelor degree… more
- Stanford University (Stanford, CA)
- …Research Coordinator Associate to perform duties related to the coordination of clinical studies . Coordinate moderately complex aspects of one or more ... Clinical Research Coordinator Associate **School of...clinical studies . Work under close direction of...capacity and willingness to learn about various aspects of clinical research (patient recruitment, coordination of study … more
- Stanford University (Stanford, CA)
- …endowments. The CRCAs will perform duties related to the coordination of health services clinical studies focusing on improving clinical cancer care delivery ... Clinical Research Coordinator Associate (Fixed-Term: 12...by coordinating moderately complex aspects of Dr. Patel's ongoing clinical studies and work under close direction… more
- Abbott (Alameda, CA)
- …+ Participate in study start up activities. + Assist with shipping study devices and supplies to clinical sites. + Perform study device ... *This role is 100% onsite in Alameda As the Clinical Research Associate I you will ensure...needed. + Proactively and effectively communicate the status of clinical studies to management. + Participate in… more
