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Job Description Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator in our New Jersey location. The ideal candidate will possess prior clinical research trial experience, phlebotomy skills, fluent in spanish and englis...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Research experience, preferred.

Senior Research Coordinator - Obs/Gyn. We are seeking a Senior Research Coordinator to join our team. Experience in OB/GYN or womens health research, proficiency with REDCap, Qualtrics, EPIC, and strong interpersonal skills.

The Clinical Research Coordinator I (CRC I) is responsible for independently coordinating simple to moderately complex clinical research studies, including registries, retrospective data reviews, and long-term follow-up studies. The role of a Clinical Research Coordinator may support task-oriente...

The Senior Research Coordinator will be responsible for initiating, coordinating and managing research studies conducted within the Department of OB/GYN with focus on the SMART-BP randomized clinical trial. Ensures the accurate execution of research protocols in accordance with Good Clinical Prac...

ATTAIN Statewide Coordinator, the ATTAIN Lab Coordinator will provide on-site and remote coordination and facilitation of activities contained in the ATTAIN lab. The Research Foundation for The State University of New York (RF) is the largest comprehensive university-connected research foundation...

This range is provided by Brooklyn Clinical Research. The Patient Recruitment Coordinator (“PRC”) plays a crucial role in our mission by promptly connecting with potential trial participants and acting as the initial facilitator of participant interactions. Clinical research experience is a plus

As a Research Coordinator, you will be an integral member of our research team, and support the conduct of an NIH-funded randomized trial to investigate the effects of an information-sharing intervention on cardiovascular health in women undergoing mammography. The Center for Behavioral Oncology ...

Due to demand, we are now accepting applications for personnel to participate in our local in-person and nationwide remote research studies. Health Issues (Research for cures and new medications to treat ailments). Upon successful completion of the research study your compensation will be issued ...

The Clinical Research Coordinator will support various research studies, encompassing government, private, and pharmaceutical initiatives. Assist with Research Billing Review (RBR) for research projects. Contribute to short-term projects and provide cross-coverage to various research team members...

Part-time Research Study Personnel (Pay up to $790/wk. Due to demand, we are now accepting applications for personnel to participate in our local in-person and nationwide remote research studies. Health Issues (Research for cures and new medications to treat ailments).

The Clinical Research Coordinator Bilingual Cantonese/English (CRC Bilingual Cantonese/English) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts routine and standardized human subjects ...

Upon successful completion of the research study your compensation will be issued via a Check, Paypal, Visa gift card or other form of compensation. Part-time Research Study Personnel (Pay up to $790/wk. Due to demand, we are now accepting applications for personnel to participate in our local in...

Wolfe Research is a mentoring shop promoting professional growth; we provide motivated candidates the opportunity to explore a career in Equity Research by providing mentors, group and individual career development sessions, and the opportunity to develop a career as a Research Associate in due t...

Upon successful completion of the research study your compensation will be issued via a Check, Paypal, Visa gift card or other form of compensation. Part-time Research Study Personnel (Pay up to $790/wk. Due to demand, we are now accepting applications for personnel to participate in our local in...

In the role of Research Coordinator, the employee will be responsible for the following:. In order to effectively represent the Company and communicate with clients, a Corbet's Research Coordinator should possess the following attributes:. A Corbet's Research Coordinator is to provide ongoing sup...

National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protoco...

SOCRA-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 Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related ex...

ClearView is looking for a highly motivated individual who wants to work in the healthcare industry to join our market research team, Expert Research Solutions, as a Primary Research Coordinator. The Primary Research Coordinator will be responsible for leveraging our network of expert physician a...

The 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 related to clinical research studies including but not limited to: answering phone calls, screen...

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 research activity. Contributes to developing educational materials and educates the community and o...

The 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 with the Oncology Clinical Research Nurses (CRNs), Oncology Clinical Research Coordinators (CRCs), D...

The 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 senior clinical research staff. Conducts routine and standardized human subjects research using app...

Reports enrollment and study progress to the research team at research meetings. Minimum 1 year experience in: (1) working in a human subjects research setting (psychology/ psychiatry preferred); (2) experience working on an NIH funded project. Other relevant experience include: (3) success in re...

Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff. The Clinical Research Coordinator will work in...

The 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 senior clinical research staff. Conducts routine and standardized human subjects research using app...

Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff. Clinical Research Coordinators at the Depressi...

Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff. The Clinical Research Coordinator will also wo...

The 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 related to clinical research studies including but not limited to: answering phone calls, screen...

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 routine and standardized human subjects research using appropriate research or interview techniq...

The Research Program Coordinator II manages activities associated to research projects, including training, supervision of staff, grant and budget preparation, data management and statistical analysis with adherence to applicable regulations. The Research Program Coordinator II develops study pro...

A Clinical Research Coordinator (CRC) I position is currently available to support our Myeloproliferative Neoplasms Program within the Tisch Cancer Institute. Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants...

The 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 senior clinical research staff. Conducts routine and standardized human subjects research using app...

The 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 related to clinical research studies including but not limited to: answering phone calls, screen...

Previous research coordinators have gone onto some of the country's top schools. Enable national participation in remote research studies via mapping of clusters, surveys, and video conferencing. Help conduct clinical assessments of research participants.

The 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 senior clinical research staff. Conducts routine and standardized human subjects research using app...

The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout the conduct of clinical studies on various existing and upcoming protocols. Understands the princ...

The 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 related to clinical research studies including but not limited to: answering phone calls, screen...

The 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 senior clinical research staff. Conducts routine and standardized human subjects research using app...

Experience in clinical research, clinical operations, or billing compliance.

The 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 Research Coordinator performs study coordination tasks under the direction of the investigator and works...

Experience in clinical research, clinical operations, or billing compliance.

The Addiction Institute of Mount Sinai is looking for a Clinical Research Coordinator I that assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities related to clinical research studies ...

At least 2 years' experience in medical field or experience as a Clinical Research Coordinator, Study Coordinator, Data Manager, or similar role in clinical research. A Clinical Research Coordinator (CRC) II position is currently available within the Medicine Clinical Trials Office. Under the sup...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Research experience, preferred.

As the OTS comprises specialists from two institutions (including HSS and New York-Presbyterian Hospital), the CRC will be responsible for coordinating OTS research at both institutions, providing ongoing research support at all stages of research to all OTS Orthopaedic surgeons and fellows, and ...

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 ...

Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff. Assists in the activities related to clinical ...