- Actalent (Virginia Beach, VA)
- …trials at the site. + Work under the supervision of the Principal Investigator (s), exercising excellent clinical judgment in patient monitoring and care. + Maintain ... daily contact with the Principal Investigator (s) for recruitment activities, study start-up, and general communication. + Execute the protocol and ensure that all… more
- IQVIA (Houston, TX)
- …to clinical trial sites and review clinical practice topics as requested by the investigator or referring sites. + Act as the point of contact with thought leaders ... for investigator -initiated study (IST's) ideas within company pipeline assets. +...respective requirements of the customers are met. Reports of drug risks are sent in writing directly to the… more
- University of Utah (Salt Lake City, UT)
- …organizations, and government agencies. Work under the direction of the Primary Investigator (PI). **Learn more about the great benefits of working for University ... and government agencies. Works under the direction of the Primary Investigator (PI). Requires moderate skill set and proficiency in discipline. Conducts… more
- Taiho Oncology (Princeton, NJ)
- …and issues. + Oversee systems to track projects including all study, investigator and ethical review board information, patient recruitment activity, and financial ... specific requirements and industry standards. + Verify that the investigator follows the approved protocol, training and all GCP...Work with internal and external functional teams to ensure drug accountability is managed at study sites and that… more
- University of Miami (Miami, FL)
- …to protocol requirements, UM and department policy. + Distributes study drug materials according to practice standards and clinical credentials as delegated ... by the Principal Investigator . + Monitors, documents, reports, and follows-up on study...implementing protocol amendments under direct supervision of the Principal Investigator . + Assists with study orientation and protocol related… more
- Geisinger (Wilkes-Barre, PA)
- …adverse experiences and compliance with study protocols. + Administers and monitors study drug as directed by the investigator and clinician. + Performs triage ... lab results and reports all findings to the principal investigator . + Informs principal investigator of all relevant patient care issues and activities within… more
- Cedars-Sinai (Beverly Hills, CA)
- …trial budgets for industry, National Institutes of Health (NIH), and investigator -initiated clinical research. Evaluates research protocols to assess resource needs, ... procedures, clinical research staff time, investigator time, and costs from ancillary departments. Determines cost...all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. **Primary… more
- University of Utah (Salt Lake City, UT)
- …control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in ... medical devices monitored and/or procedures followed. 13. Assists the Principal Investigator in the development of study protocols **Clinical Research Coordinator… more
- AdventHealth (Orlando, FL)
- …for the patient, while adhering to the conduct of industry-sponsored and investigator -initiated clinical trials in accordance with trial protocols, Food and Drug ... the initiation and completion of clinical research studies. Promotes Principal Investigator (PI) oversight by advising the PI, sub- investigator (s), Lead… more
- University of Pennsylvania (Philadelphia, PA)
- …requirements, and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report ... contribute to study-related meetings, including but not limited to Investigator Meetings, Site Initiation Visits, Intermediate Monitoring Visits, Close-out Visits,… more