Head of Clinical Research - New York, NY

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. ...

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 and all additional protocol amendment trainings. · Adherence to ALCOA-C Standards with all clinical trial docume ...

The Clinical Research Coordinator monitors data management and regulatory aspects of clinical-trial operations.We help improve therapeutic efficacy and safety for all individuals. · ...

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

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 ...

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 ...

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. · ...

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 ...

Clinical Research Associates are responsible for coordinating and overseeing the execution of studies and clinical trials. · ...

Clinical Research Associates (CRAs) coordinate clinical trials under pharmaceutical companies' guidance. · Participating in study team meetings. · ...

We are supporting a growing clinical research site network in hiring Clinical Research Coordinators to support late-phase, industry-sponsored clinical trials across psychiatric and neurological indications. · ...

We are seeking a dedicated Clinical Research Coordinator to join our team.The ideal candidate will be responsible for coordinating and overseeing clinical research studies ensuring compliance with protocols regulations and ethical standards. · The Clinical Research Coordinator wi ...

We are seeking a Certified Clinical Research Coordinator (CCRC) to join our growing clinical research site on a part-time basis (one day per week). This role is ideal for an experienced coordinator who values high-quality research, operational excellence, and schedule flexibility ...

We are seeking an experienced Clinical Research Coordinator with phlebotomy experience to support industry-sponsored clinical trials with active investigational products. · 2+ years of clinical research coordination experience (industry-sponsored IP required) · Phlebotomy experie ...

Manages clinical research projects and oversees staff and patient care delivery. · ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. · Lensa part ...

Join IMA Clinical Research and be part of studies that change lives. · ...

Job summary · The Clinical Research Coordinator manages clinical trials conducted through the Clinical Protocol & Data Management Office. This position reports directly to the Clinical Research Manager of the specific disease site this incumbent is assigned to.The above hiring ra ...

This entry-level position provides coordination and administrative support for clinical research projects, · Clinical Coordination: Screen participants for study eligibility, enroll them accurately in various databases. · Data Coordination: Enter data in CRFs, databases or EDCs. ...

The opportunity to lead clinical research and evidence strategy for Twofold Health as a senior clinician-research leader who can bring rigor, relevance, and speed. · We help clinicians stay on top of patient context translate visits into actionable follow-up run tighter care loop ...