SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Coordinator will conduct study operations and activities of designated studies, including those that are part of the ...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human...
Clinical Research Coordinator III A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Occasionally attending out-of-town Investig...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
Job Description: Studies Coordinator – Photoprotection. We are looking for a detail-oriented and proactive Studies Coordinator to join our Photoprotection – US Clinical & Instrumental Evaluation Intelligence Team. Contact Contract Research Organizations (CROs) to coordinate testing timelines, manage...
The Research Coordinator coordinates and performs all the associated duties associated with coordination and implementation of the conduct of clinical research trials and projects. A day in the life of a Research Coordinator at Hackensack Meridian Health includes:. Serves as primary study coordinato...
Compliance, Research and Medical Coordinator. The Compliance, Research and Medical Coordinator is responsible for managing the compliance functionality to support the OrthoFeet documentation procurement program, and for managing it therapeutic shoe fitting service, Fit to Go. Point of contact for re...
PCR CRCNJ seeks a Clinical Research Coordinator who will be responsible for managing the day-to-day operations of assigned clinical trials, assisting in project planning, and ensuring that pre-established work scope, study protocol, and regulatory requirements are followed. The Clinical Research Coo...
Clinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations. ...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Coordinator will conduct study operations and activities of designated studies, including those that are part of the ...
Rutgers University- Newark (RU-N), an urban public research university and anchor institution, located in Newark, New Jersey, a city of promise is seeking a Research Project Coordinator I, Career Outcomes & Assessment. In conjunction with a graduate coordinator, serves as the primary researcher in t...
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human...
As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health. ...
Title: Compliance, Research and Medical Coordinator. The Compliance, Research and Medical Coordinator is responsible for managing the compliance functionality to support the OrthoFeet documentation procurement program, and for managing it therapeutic shoe fitting service, Fit to Go. Point of contact...
The Clinical Research Coordinator III will serve as a member of the Clinical Research team. Aligned with Rutgers University–New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and re...
Required Skills: Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. Join us and help clients adapt to evolving requirements in ...
Rutgers The State University of New Jersey is seeking a motivated Temporary Research Coordinator for the Department of Pediatrics at Rutgers Biomedical and Health Sciences. The primary purpose of the Temporary Research Coordinator will be to work mostly at the CRC at the Child Health Institute and t...
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human...
Clinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations. ...
Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within rep...