Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. We have an exciting opportunity to join o...

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 se...

Individual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine. Contributes to the preparation of artic...

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 se...

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 complianc...

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 complianc...

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...

A Clinical Research Coordinator II position is currently available within the Medicine Clinical Trials Office. Under the supervision of the clinical research manager, the coordinator maintains procedu...

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 se...

Individual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine. We have an exciting opportunity to join...

Under general supervision with latitude for independent judgment and initiative, assists in the planning, organizing and coordination of research activities for the Network. At least two (2) years' ex...

The 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...

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 se...

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...

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 se...

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 se...

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...

This includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, p...

The 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...

This includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, p...

The 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...

Clinical Research Coordinators at the Depression and Anxiety Center for Discovery and Treatment (DAC) are responsible for research, clinical, and administrative tasks related to conducting a given stu...

Coordinates the development of forms, questionnaires and the application of research techniques, assists in writing procedure manuals, reviews journals, abstracts and scientific literature to keep abr...

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred...

The Coordinator drives recruitment and assists research participants on clinical research studies, coordinates and schedules participant clinic visits, and serves as principal administrative liaison f...

The 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...

This position is for a full-time Clinical Research Coordinator I (CS02) in the Eating and Weight Disorders Program. This position requires a candidate with a master's degree, trained in psychotherapy ...

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...

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 PI and ...

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...

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...

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...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...

Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...

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...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...

Assist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.

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 inv...

The 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 ...