Clinical Research Coordinator

SUMMARY

The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities.

USRC has a research Partnership with the principal investigator (PI) and their physician practice.

The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI.

The CRC will work collaboratively with the principal investigator (PI), the Sr.

Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations.

The CRC will assist the PI in protecting the rights, safety and welfare of all study participants.

Essential Duties and Responsibilities include the following.

Other duties and tasks may be assigned.



* Coordinate all aspects of participant care from screening through study completion as defined by the protocol and PI delegation.


* Ensure and document that the informed consent process has occurred properly according to the Code of Federal Regulations (45 CFR part 46).


* Assist in the process of maintaining and updating each study participant's source records, including collection of medical history, assessment of eligibility and documentation of all study related procedures and relevant information.


* Promptly report adverse events, protocol deviations and unanticipated problems involving risk to human subjects or others to the PI, the Sponsor, the IRB and in accordance with the Federal Code of Regulations (21 CFR 312), with assistance as applicable.


* Ensure thorough, individualized, protocol-based study subject education on all study processes including but not limited to informed consent, study participation obligations, appropriate use of investigational product (IP), IP side effects and safety, communication with study staff and research rights.


* Provide timely and accurate exchange of participant information with the PI and research team as it pertains to study conduct and patient safety.


* Adhere to the Health Insurance Portability and Accountability Act (HIPAA Privacy Rule) and protect participant confidentiality at all times.


* Dispense, administer and instruct participants on proper use of the investigational product (IP) in accordance with the protocol, coordinator's scope of practice and at the direction of the PI, with assistance as needed.


* Collaborate with the USRC clinical team.

Participate in trial implementation, and ensure compliance with the study protocol by our clinical partners, with assistance as needed.


* Perform accurate and timely data collection, source documentation, and entry into the USRC databases and sponsor Case R...