Creates, generates and analyzes statistical reports to track and measure various clinical functions.
The Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts...
read moreUnder general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Oversees data collection, processing, storage, inventory and...
read moreThe Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits and serves as principal administrative liaison fo...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...
read moreThe Clinical Research Coordinator II is responsible for the implementation of assigned study activities, including activation, maintenance, and closure processes. Assists with training of new Clinical...
read moreThe Clinical Research Coordinator is an active participant in the coordination of critical care and resuscitation research studies from research planning to completion of studies. The Clinical Researc...
read moreThe Oncology CRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of the CTO management/leadership and works closely wit...
read moreThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...
read moreThe Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subject...
read moreMinimum of 1 year experience as a Clinical Research Coordinator. We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our team in Livingston, NJ. Maintain comprehensive...
read moreWe are seeking an experienced Clinical Research Coordinator I (CRC I) for research projects examining risk and protective factors for cognitive, sensorimotor, and affective outcomes in persons with mu...
read moreThe Clinical Research Coordinator will also work closely with other Clinical Research Coordinators and Study Clinicians to adhere to clinical protocols conducted with study participants focused on sub...
read moreAre you passionate about clinical research and patient care? Do you have strong communication and medical research kills but have not been able to apply them? Are you looking to become a dermatologic ...
read moreCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Brooklyn Clinical Research provided pay range. To support this objective...
read moreCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. This range is provided by Brooklyn Clinical Research. To support this ob...
read moreUnder general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Mentors, trains and reviews the work of less experienced cli...
read moreThe Clinical Research Coordinator acts as a liaison among principal investigators, sub-investigators, clinical research nurses, and regulatory specialists, ensuring smooth communication and compliance...
read moreCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. To support this objective, we establish clinical research sites in dense...
read moreCompany history: Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. To support this objective, we establish clinical research sites in dense...
read moreTitle: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...
read moreTitle: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...
read moreClinical Research Coordinator analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Mentors, trains and reviews the work of less experienced ...
read moreCollect and manage clinical trial data from different sources, like forms and electronic systems. Check for errors or mismatches in the data and work with the research team to fix them. Review data to...
read morePCR 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 w...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreThe Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. The Clinical Research Coord...
read moreThe Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...
read moreObtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies ...
read moreClinical Research Coordinator I. Experience in clinical research, clinical trials, or a medical-related profession is highly preferred. Clinical Research Coordinator I.
The Department of Population Health Science and Policy is seeking a full-time Clinical Research Coordinator II (CRC) to work with Dr. Proficiency working with research program tools such as RedCap and...
read moreClinical Research Coordinator I. Experience in clinical research, clinical trials, or a medical-related profession is highly preferred. Clinical Research Coordinator I.
Trains clinical staff on study protocols and procedures and supervises the Clinical Research Unit (CRU) staff when the principal investigator or sub-investigators are not present to direct clinical re...
read moreThe Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...
read moreThe Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCPs) in the process of screening, enrolling and closely monitoring clinical research study subject...
read moreThe Clinical Research Coordinator coordinates and assists with the daily operations of clinical research studies. The Coordinator drives recruitment and assists research participants on clinical resea...
read moreThe Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits, and serves as principal administrative liaison f...
read moreWe are seeking a highly organized and dedicated Clinical Research Coordinator to join our research team in the. We have an exciting opportunity to join our team as a Clinical Research Coordinator. Ens...
read moreThe Clinical Research Coordinator I will be the point person for multiple research projects and help establish, track, oversee, and monitor neuroimaging acquisition protocols, data transfer, and data ...
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