- Kedplasma (Fort Lee, NJ)
- …may have! **Job Scope / Job Mission** _We are seeking an experienced and highly motivated Senior Clinical Trial Assistant (CTA) to join our Clinical ... Operations team. This role is pivotal in supporting clinical trials from initiation to completion, ensuring...The ideal candidate will bring a combination of proven clinical trial support expertise, ability to lead… more
- IQVIA (Mooresville, NC)
- …division, IQVIA Laboratories . IQVIA Laboratories is a leading global clinical trial laboratory services organization providing comprehensive testing, project ... **Job Profile Summary** This Sr QA Auditor will work with...management, supply chain, biorepository and specimen management, and clinical trial sample and consent tracking solutions.… more
- Chiesi (Cary, NC)
- Senior GCP Auditor Date: Feb 8,... Laboratories, Trial Master Files, investigational sites, clinical service providers supporting clinical trials ... group to be awarded **B Corp Certification** , a recognition of **high social and environmental standards.** We are...or Contract Research Organization (CRO) + 4+ years in clinical trials management on investigational medicinal products… more
- University of Rochester (Saunders County, NE)
- …of the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE: The Clinical Trials Project Manager II is responsible for leading ... of over 600 community sites. Under oversight of the Sr . Clinical Research Project Manager, the CRPM...multiple studies' day-to-day operations, carry out project management for clinical trials run through the URCC NCORP… more
- Bristol Myers Squibb (Princeton, NJ)
- …goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Auditor in GIA will work in a team environment to plan ... and key third-party outsourcing arrangements. Throughout the audits, the Senior Auditor will have the opportunity to...unique perspectives in an inclusive culture, promoting diversity in clinical trials , while our shared values of… more
- Edwards Lifesciences (Irvine, CA)
- …management skills with ability to drive achievement of objectives * Relevant clinical trial experience in heart valve disease, coronary artery disease, ... various teams to influence decision-making for a product's entire lifecycle. As the Sr . Principal Quality Engineer, you will be responsible supporting the health of… more
- Johns Hopkins University (Baltimore, MD)
- …responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to ... clinical care vs research costs for participation in clinical trials and clinical research...clinical care guidelines. This position reports to the Sr . Director Research Administration **Specific Duties & Responsibilities** +… more
- MD Anderson Cancer Center (Houston, TX)
- …data as assigned. **Protocol Administration Responsibilities** Ensures the conduction of assigned clinical trials is in accordance with Good Clinical ... in hospital account reconciliation and to facilitate compensation from sponsors of clinical trials as assigned. **Protocol Patient Management** Assist research… more
- University of Rochester (Rochester, NY)
- …operation and evaluation of divisional procedures required to ensure quality clinical trial research within the Division of Pediatric Hematology/Oncology. ... IRB standards. The regulatory agencies include the University IRB, clinical trials office, and the FDA. Ensure...Preferred Qualifications - 2 years prior experience as a Senior Health Project Coordinator - Certified Clinical … more
- MD Anderson Cancer Center (Houston, TX)
- …data supervisor/manager assists the investigator in the overall conduction of assigned clinical trials * Participates in Site Initiation Visits (SIVs), ... and protocol meetings * Ensures the conduction of assigned clinical trials is in accordance with Good...necessary functions when absent * Schedules internal and external auditor /monitor visits for a team, section or department *… more
- Weill Cornell Medical College (New York, NY)
- …management of clinical research studies. **Job Responsibilities** + Coordinate clinical trials in compliance with federal regulations, GCP guidelines, and ... sponsoring agencies and external sites. + Coordinates site visits and audits of clinical trials in conjunction with all pertinent staff, including: the monitor/… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …Product QA) quality systems, GCP & PV quality systems, the safety of clinical trial participants, the veracity of study data, compliance with related ... the quality of commercial products and investigational medicinal products, the safety of clinical trial participants, and/or study data veracity, to identify and… more
- Astellas Pharma (Westborough, MA)
- …a diverse range of disease indications, ranging from macular degeneration (currently in clinical trials ) and other ocular indications to vascular and autoimmune ... M-TC's cGMP Cell Therapy Manufacturing facility as the products move through clinical trials and commercialization. This position is responsible for… more