Position Overview :
In this role you will ensure IRB approved protocols are implemented and followed; execute the
informed consent process and monitor patient status and safety; collect and organize research
data; schedule and conduct study-specific training and site in-services to study related staff on
new or amended protocols, and educate patients and their families about treatments and
possible side effects. The Clinical Research Coordinator must also be able to perform clinical
tasks.
Responsibilities : Site preparation.
Site preparation.
Obtaining informed consent, patient screening and recruitment.
Patient enrollment, and conducting study visits.
Maintaining and dispensing study product and supplies.
Completing and ensuring the quality of case report forms.
Maintaining source documents
Ensuring site quality.
Maintain a thorough and meticulous working knowledge of protocol schemas and requirements.
Collaborate with physicians to maintain strict protocol adherence and serve as a resource for members of staff.
Writes patient information sheet for clinical studies for submission to IRB, as well as complete the necessary documents for IRB admission in a timely fashion.
Participate in the development and implementation of patient educational materials.
Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well a complete the necessary documents for IRB submission in a timely fashion.
Review research and administrative documents to determine action items, prioritizing and tracking action items.
Responsible for completion, submission and tracking of regulatory documents to the IRB.
Maintain and update research fund accounting files, research billing, budgets and transfer of funds.
Respond to correspondence, data and informational requests.
Analysis of statistical, resource, performance and budget data and generation of reports.
Qualifications :
1-2 years of Clinical Research Coordinator (CRC) experience or relevant experience
Clinical Research Coordinator- 232165
The Clinical Research Coordinator must also be able to perform clinical. Clinical Research Coordinator (CRC) experience or relevant experience. Maintain and update research fund accounting files, research billing, budgets and transfer of funds. Writes patient information sheet for clinical studies f...
Clinical Research Coordinator I
Master's degree in a related field with 2 years of experience working as a clinical research coordinator or research project manager, and/or experience in research data collection and/or collaboration with interdisciplinary teams or experience in doing research with older adults. Under grant funding...
Clinical Research Data Coordinator I
In this role, the Clinical Research Data Coordinator I collaborates with study Investigators, Clinical Research Coordinator(s) (CRC), study sponsors, and other research and clinical team members in the conduct of Phase I-IV industry-sponsored, grant funded (federal or other grants), and/or investiga...
Clinical Research Coordinator
The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI), Sub-Inv...
Clinical Research Coordinator II -RN
Schedule:** Full-Time/Day **Shift** : Monday-Friday **The role you’ll contribute:** The Clinical Research Coordinator II RN (CRC-II RN) serves the AdventHealth Research Institute (AHRI), under limited supervision, to plan, coordinate, evaluate and perform the nursing care of participants and collect...
Clinical Research Coordinator (20 hours/week)
Clinical Research Coordinator (Part-time, 20 hours per week). Coordinates, implements and completes clinical research studies or clinical trials by assisting with IRB submissions. Radiology Department will serve the Radiology Enterprise's efforts on all research endeavors. Position is based in Orlan...
Clinical Research Coordinator Radiology
Nemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team based in Orlando, FL. Coordinates, implements and completes clinical research studies or clinical trials by assisting with IRB submissions. Radiology Department will serve the Radiology Enterprise's efforts...
Clinical Research Coordinator
If you're a Clinical Research professional ready to take the next step in their career and work in. Coordinates the implementation of multiple complex clinical research protocols. Develops SOPs and templates with guidance from the PI and/or Clinical Research Manager. We are looking for someone to ta...
Assistant Clinical Research Coordinator
The role involves assisting the Clinical Research Coordinator and Investigator with various clinical study activities, providing comprehensive Quality Control support for the completion of source documents and CRFs for clinical trials. Job Title: Assistant Clinical Research Coordinator. Experience i...
Project Manager - Land Development
Land Development Project Manager. Manages the project scope, cost, schedule, mitigate risks and ensures every team member contributes to the project delivery process. The primary focus of this role will be to manage and deliver multiple complex land development projects from preliminary planning thr...