Associate Principal Scientist, Clinical Research - Rahway

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. · ...

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 ...

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. · ...

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 seeking committed, skilled, and customer-focused individuals to join our winning team as Clinical Research Associates II. · ...

+Job summary · Clinical Research Associate II · +Interact with personnel from study Sponsors, investigational sites, vendors, and Everest functional groups to enable quality and on-time execution of clinical trials in compliance with ICH-GCP and relevant local regulations. · Iden ...

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 ...

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. ...

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. · ...

Soterix Medical, Inc. is seeking a Clinical Research Coordinator (CRC) to work closely with the research staff to conduct clinical trials in the field of neuromodulation, · ...

· Our team members are the heart of what makes us better. · We help our patients live better healthier lives — and we help one another to succeed. · The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical ...

The Clinical Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the therapeutic area. · The successful candidate will be responsible for maintaining a strong scientific fund of knowledge by staying up ...

The Senior Director has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. · Specifically, · Evaluating pre-clinical and transl ...

The Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology.With a focus on late-stage development, the Clinical Director will manage the entire cycl ...

The Clinical Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines.The Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, ex ...

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the therapeutic area.The successful candidate will be eligible for annual bonus and long-term incentive if applica ...

The Clinical Director has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, they will manage the entire cycle of clinical development including st ...

+ Job summary: The Senior Director has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. · + Qualifications:M.D or M.D./Ph. · Must ...