Clinical Research Assistant

* On Site position.


* Office Hours are Monday-Friday 8am-4:30pm.

PURPOSE AND SCOPE:

Provides administrative and clinical support for the implementation and conduct of clinical trials under the direct supervision of the

Principal Investigator (PI), Director, and other site personnel as applicable.

Responsible for the collection and submission of

regulatory documents, performance of study specific procedures, regulatory reporting requirements as instructed by the PI and

governed by Good Clinical Practice (GCP) and ICH guidelines, and assisting with ongoing study activity.

 

PRINCIPAL DUTIES AND RESPONSIBILITIES:


* Assists with obtaining and preparing regulatory/essential documents throughout the duration of a study including, but not limited to, FDA 1572, CVs, professional licensure, financial disclosure forms and IRB submission forms.


* Under close supervision, ensures documents and forms are compiled and submitted in a timely manner to the CRO, study sponsor or IRB as applicable.


* Assists with maintaining constant communication with Institutional Review Boards, study sponsors, dialysis facility, practice and field staff as necessary to ensure timely study start-up or the effective and efficient progression of the study.


* Assists with the contracting process, document preparation and execution as required during study start-up activities and throughout the duration of a study.


* Under close supervision, interfaces with potential study subjects for the purpose of promoting participation in research studies.


* Assists with the screening of subjects for participation eligibility using inclusion/exclusion criteria as outlined in the study protocol and under the direction of the PI.


* Assists with and documents the obtaining of informed consent according to GCP.


* Assists with the timely and accurate data entry of study specific data into case report forms.


* Assists with addressing and resolving study sponsor questions, concerns, and queries in accordance with timelines established by the study sponsor.


* Processes and ships study specific lab specimens as directed by the PI.


* Performs study specific procedures at protocol directed intervals under the supervision of the PI.


* Provides general support for research projects as directed by the PI, Director, or other site personnel.


* Obtains and updates essential documents for specific studies, as necessary.


* Attends clinical research-related training as required.


* Assists with study close-out activities as directed by PI.


* Completes the clinical trials management system and electronic/paper case report forms in an accurate and timely manner.


* Escalates issues to supervisor for resolution, as deemed necessary.


* Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and


* federal laws and regulations.


* Assists with variou...