- System One (Boston, MA)
- Title: Clinical Trial Protocol Coordinator Location: Boston, MA Hybrid schedule Start Date: ASAP Duration: 6 Month Contract-to-Hire Hours: Mon-Fri, ... in the administrative day to day project activities. + Advise sites on protocol conduct, interpretation of protocols and ensures resolution of issues as applicable.… more
- UCLA Health (Los Angeles, CA)
- … Coordinator contributes to the overall operational management of clinical research/ trial /study activities fromdesign, set up, conduct, through closeout. ... and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal...research budgeting process to assist with the preparation of clinical trial budgets. * Working knowledge of… more
- University of Southern California (Los Angeles, CA)
- …Nurse and has a strong interest in clinical research. The role of the protocol coordinator is a diverse one. This person works independently, yet is able to ... Protocol Coordinator (Research Nurse)Apply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Protocol -… more
- Vitalief (New Brunswick, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management. and other clinical trial activities for solid tumor, high… more
- Guidehouse (Bethesda, MD)
- **Job Family** **:** Clinical Trial Operations (Digital) **Travel Required** **:** None **Clearance Required** **:** Ability to Obtain Public Trust **What You ... Bethesda or virtual meetings, including weekly CTU staff meetings, protocol development meetings, research coordinator forum meetings,...Minimum of Two (2) years of experience in a clinical trial or clinical research… more
- Guidehouse (Bethesda, MD)
- **Job Family** **:** Clinical Trial Operations (Digital) **Travel Required** **:** None **Clearance Required** **:** Ability to Obtain Public Trust **What You ... Will Do** **:** We are currently searching for a Clinical Research Protocol Navigator. The primary role...+ At least (2) years of experience in a clinical trial or clinical research… more
- University of Pennsylvania (Philadelphia, PA)
- …the accuracy of all study documentation. The coordinator will oversee 2 or more clinical trial ensuring that the integrity of the protocol is maintained, ... of all study documentation. The coordinator will oversee 2 or more clinical trial ensuring that the integrity of the protocol is maintained, all data… more
- University of Pennsylvania (Philadelphia, PA)
- …in patient safety, protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy (IDS) to ... research performed. He/she will be responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data entry, subject… more
- MD Anderson Cancer Center (Houston, TX)
- …to the protocol team. ** Protocol Submissions:** + Prepares and reviews clinical trial documents for submission of new and amended or modified documents ... ** Coordinator , Clinical Studies - Genitourinary Medical... protocol , contract, and budget approval that affect clinical trial operations (activation, amendments, etc.). +… more
- University of Pennsylvania (Philadelphia, PA)
- …preferred qualifications for CRC-B/C: + Bachelor's degree, a minimum of 2 years clinical trial experience, along with outstanding references. + Must have a ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Neurology)... will take an active role in preparation of trial audits and inspection. The coordinator will… more
- University of Pennsylvania (Philadelphia, PA)
- …entry, subject visits and follow-up and trial documentation. Job Description Clinical Trials Coordinator B: This individual will work under general ... products and various sponsors. He/she will be responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data… more
- Georgetown Univerisity (Washington, DC)
- …a manner that they may not experience otherwise as a patient. Per the requirements of each clinical trial protocol , the CRC2 is required to be the main point ... entire study visit for each patient, ensuring that the protocol is followed, which requires an in-depth understanding of...Degree and 5 years' minimum work experience as a Clinical Trial Coordinator or … more
- Georgetown Univerisity (Washington, DC)
- …a manner that they may not experience otherwise as a patient. Per the requirements of each clinical trial protocol , the CRC2 is the main point of contact for ... conducting the entire study visit, ensuring strict adherence to protocol - which necessitates an intimate understanding of each...at least 5 years of work experience as a Clinical Trial Coordinator or … more
- Actalent (Hialeah, FL)
- …participant adherence to protocol Skills: Chart review, Pre-screening patients, Clinical trial , EDC, Patient recruitment Top Skills Details: Chart ... of reports, documents and correspondence for regulatory agencies, participating clinical trial sites and for internal purposes....with several principal investigators * Serve as back up coordinator to other clinical trials * Completes… more
- ICON Clinical Research (Salisbury, NC)
- …progress notes, as well as phone screening participants + Completes training on Clinical Trial Management System and maintains proper skills to update database, ... Coordinator I_ **_Location_** _: Salisbury, NC_ **Summary:** The Clinical Research Coordinator I will ensure the...with volunteers, and participates in patient education regarding the clinical trial process and provides specific … more
- Georgetown Univerisity (Washington, DC)
- …with Clinical Research Coordinators. + Provide patient education about clinical trial participation, treatment, potential side effects, and required testing. ... inquiry and making a difference in the world. Requirements Clinical Research Nurse Coordinator I, Center for...with Data Manager(s) to assure the documentation for the clinical trial is complete and accurate; assist… more
- Baptist Memorial (Memphis, TN)
- …study opening. The CTPC must have experience in clinical trials and protocol start-up activities to work with trial Principal Investigator (PI) and research ... Summary This Clinical Trials Pipeline Coordinator (CTPC) position...the management and implementation of cooperative group and industry clinical trial protocols at Baptist Clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …and various sponsors. S/he will be responsible for all aspects of clinical trial coordination. The coordinator will assist physicians/investigators ... coordinator will execute and ensure adherence to the protocol and Good Clinical Practice, while taking...study. Notify PI, managers, sponsor of any deviations from protocol or adverse events. Assure reported trial … more
- MD Anderson Cancer Center (Houston, TX)
- …* Consults with principal investigator (PI) and/or Mgr., Clinical Protocol Administration regarding ongoing clinical trial assignments. Works ... **SUMMARY** The primary purpose of the Senior Coordinator , Clinical Studies position is to...metrics for the purpose of grant submissions, budget creation, clinical trial evaluations, protocol review… more
- Cedars-Sinai (Los Angeles, CA)
- …projects. + Assists Research Grant Specialist with creating and negotiating industry-sponsored clinical trial budgets. + Assists Research Grant Specialist with ... financial post-award monitoring/accounting of clinical research projects. + Negotiates clinical trial agreement payment terms with industry sponsors +… more