- Parexel (Glendale, CA)
- …enrollment of study participants. Contributes to the development and implementation of study/ research objectives. + Assess, monitor , record, and report patient's ... **Parexel Early Phase Clinical Unit** supports the development of innovative new...to, IV, IM, SC, PO, Topical, Inhalation etc. Then monitor the volunteer participants health status around the clock… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Department of Neurosurgery) Job Profile Title ... Clinical Research Coordinator C Job Description Summary...protocol + Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …innovative medicines, solutions and services in more than 110 countries and regions. The Clinical Research Associate assists in the management of the clinical ... a life science field preferred. + Typically requires 5 years of experience in clinical research , including a minimum of 2 years field monitoring experience and… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …in life sciences or related discipline. * 6+ years' experience as a Clinical Research Associate. * Extensive knowledge of trial oversight activities, GCP/ICH ... needs of the organization._ **Job Locations** _US-IL-Chicago_ **Title** _Senior Clinical Research Associate (CRA)_ **ID** _2025-2205_ **Category** _Clinical… more
- Ascension Health (Jacksonville, FL)
- …range at the time of the offer._ **Responsibilities** Coordinate administrative and clinical aspects of multiple research projects. + Collaborate with primary ... **Details** + **Department:** Research + **Schedule:** Days + **Hospital:** Ascension St....staff to plan, conduct and evaluate project protocols. + Monitor and report on progress of projects. + Assist… more
- Actalent (Madison, WI)
- Clinical Research Technician Join our Phase I Clinical Research Unit and gain hands-on experience in clinical trials. Work closely with nurses and ... venipuncture. + Collect, process, and distribute biological samples per protocol. + Monitor participant meals for dietary compliance. + Prepare rooms and equipment… more
- Ascension Health (Milwaukee, WI)
- …range at the time of the offer._ **Responsibilities** Coordinate administrative and clinical aspects of multiple research projects. + Collaborate with primary ... **Details** + **Department: Research Oncology** + **Schedule: Full Time, Days (M-F... staff to plan, conduct and evaluate project protocols. Monitor and report on progress of projects. + Assist… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... regulations, and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day...assess the safety and efficacy of investigational products and/or medical devices * Conduct site visits to determine protocol… more
- Stanford University (Stanford, CA)
- …Office. . Knowledge of medical terminology. **CERTIFICATIONS & LICENSES:** Society of Clinical Research Associates or Association of Clinical Research ... Medical Psychiatry Research Assistant(6 Month Fixed...of Medicine is seeking a 6 month Fixed Term Clinical Research Coordinator Associate to perform duties… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …training, as needed/requested. DESCRIPTION OF RESPONSIBILITIES: The WRAIR-based clinical research scientific monitoring services (Post-Approval Compliance ... EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience... + Knowledge and experience in the areas of clinical research and regulatory affairs as related… more