Director, Clinical Research - Manhasset

We are seeking a highly organized Clinical Research Coordinator to oversee clinical trials within our research facility. · Coordinate and supervise clinical trial activities in accordance with FDA regulations. · Manage patient enrollment screening monitoring follow-up ensure adhe ...

The Clinical Research Coordinator monitors data management and regulatory aspects of clinical-trial operations. · Completing all relevant training prior to study start and all additional protocol amendment trainings. · Adherence to ALCOA-C Standards with all clinical trial docume ...

DM Clinical Research is looking for an Investigator for our site in Jersey City, NJ to conduct all clinical trials according to ICH and company processes. · Ensures the medical well-being and safety of participants through safe performance and execution of studies. · ...

The Clinical Research Coordinator monitors data management and regulatory aspects of clinical-trial operations. · Completing all relevant training prior to study start · Adherence to ALCOA-C Standards with all clinical trial documentation · ...

A study manager ensures quality research is conducted at assigned investigative sites in accordance with sponsor protocol FDA Regulations ICH/GCP guidelines providing best quality data to sponsor ensuring study enrollment meets or exceed Sponsors expectations company goals are ac ...

The Site Manager's job is to 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. ...

Job summary · Clinical Research Coordinator III will ensure quality research is conducted at assigned sites in accordance with sponsor protocol and FDA Regulations. · Completing all DMCR-required training. · Conducting study subject visits and documenting procedures. · Liaising w ...

We are looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. · ...

DM Clinical Research is looking for an Unblinded Clinical Research Coordinator II to join our team in New Jersey. · ...

· Bachelor's degree required. · ...

Directs clinical research program activities to ensure goals and objectives are accomplished within prescribed time-frame and funding parameters. · ...

Directs clinical research program activities to ensure goals and objectives are accomplished within prescribed time-frame and funding parameters. · ...

Clinical research coordinator coordinates and monitors research trials; actively oversees the recruitment of study participants. · Bachelor's Degree required, · 1-3 years of relevant experience required, · ...

+Job summary++Coordinates and monitors research trials; actively oversees the recruitment of study participants.+ · May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements.Adheres to g ...

Clinical research coordinator coordinates and monitors research trials; oversees recruitment of study participants. · ...

+Candidates will coordinate and monitor research trials; actively oversee the recruitment of study participants. They may be required to perform venipuncture on study participants; collect, process, and ship specimens according to protocol and training requirements. · +Coordinate ...

Participates and assists in research and academic activities. Collaborates with all members of the research program as well as nursing, physician, house staff, · and ancillary staff related to academic activities of the department.Participates in research activities; assists the ...

Participates and assists in research and academic activities. · ...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. · ...

Clinical research coordinators oversee the day-to-day activities of clinical trials and studies. They work with researchers, doctors and patients to ensure that studies are carried out efficiently and effectively. · Coordinate the recruitment of study participants · Collects lab ...