Senior Clinical Research Associate Jobs in Butler, NJ

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site... Read More

WHY VITALIEF? Vitalief is emerging as an innovative Healthcare consulting company, focused on empowering Research and transforming Clinical Trials. As a result, we are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team... Read More

For Current Gilead Employees and Contractors: Please log onto your Internal Career Site (https://www.myworkday.com/gilead/d/inst/13102!CK5mGhIKBggDEMenAhIICgYI1A0QtgI~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job. At Gilead, we re creating a... Read More

Summary: The Clinical Research Coordinator reports to the Manager of Clinical Research and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Coordinator will perform a variety of duties involved in... Read More

Clinical Trial Associate, Study Management 23 months Remote Education / Certificates: Bachelor's degree in Life Sciences with minimum 3 or MS in Life Sciences with minimum 1+ year of relevant experience in clinical drug development. Experience Practical experience... Read More

Job Description The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of... Read More

Position Details Position Information Recruitment/Posting Title Clinical Research Coordinator III Job Category Staff Executive - Research (Laboratory/Non-Laboratory) Department NJMS-Medicine-Infectious Disease Overview New Jersey's academic health center, Rutgers... Read More

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. To ensure... Read More