Interacts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Understand, monitor, and repor...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Clinical research study point ...
read moreJoin our dynamic pulmonology research team as a Research Coordinator, where you will contribute to cutting-edge studies in cystic fibrosis, asthma, COVID, and various other pulmonary diseases. Demonst...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Understand, monitor, and repor...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. ACRP (CCRC, CCRA) or SoCRA (CC...
read moreJoin our dynamic pulmonology research team as a Research Coordinator, where you will contribute to cutting-edge studies in cystic fibrosis, asthma, COVID, and various other pulmonary diseases. Demonst...
read moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
read moreClinical Research Coordinator- Norwalk Hospital Cancer Research - Full time, 40 hours - Monday - Friday, 8:00am to 4:30pm. Functions independently in a clinical research setting and responsible for th...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Clinical research study point ...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Clinical research study point ...
read moreUnder oversight and direction from the Program Director and Department Director, the Clinical Research and Graduate Medical Program Coordinator is responsible for the day to day administrative and ope...
read moreUnder oversight and direction from the Program Director and Department Director, the Clinical Research and Graduate Medical Program Coordinator is responsible for the day to day administrative and ope...
read moreOversees the weighing and research program for designated terminals. Collaborates with regional and terminal operations teams to address personnel issues related to weight and research process complia...
read moreOversees the weighing and research program for designated terminals. Collaborates with regional and terminal operations teams to address personnel issues related to weight and research process complia...
read morePart-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. Heal...
read morePart-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. Heal...
read moreUpon 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/...
read morePart-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. Heal...
read morePart-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. Heal...
read moreUpon 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/...
read moreFunction independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporati...
read morePREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Function independently in a clinical research setting and responsi...
read moreTitle: Clinical Research Coordinator. Attend meetings with the research team to discuss study progress and results. The successful candidate will be responsible for assisting with various clinical res...
read moreTitle: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...
read moreTitle: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...
read moreTitle: Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including statistical analysis, literature reviews, manuscri...
read moreTitle: Clinical Research Coordinator. Assist in the preparation of research findings for publication in peer-reviewed journals. Attend meetings with the research team to discuss study progress and res...
read moreThe Senior Clinical Research Coordinator will primarily oversee the Spaulding-Harvard Traumatic Brain Injury Model System (SH-TBIMS), one of 16 centers nationally funded by the National Institute on D...
read moreThe Senior Clinical Research Coordinator will primarily oversee the Spaulding-Harvard Traumatic Brain Injury Model System (SH-TBIMS), one of 16 centers nationally funded by the National Institute on D...
read moreWorking with a collaborative and supportive team, you'll coordinate clinical research protocols, assist investigators in launching research studies, and ensure seamless communication within the resear...
read morePart-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. Heal...
read morePart-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. Heal...
read moreOur Clinical Research Institute in Stamford is looking for a motivated Lead Clinical Research Coordinator to help us conduct clinical trials in the Fairfield County area, primarily focusing on neurolo...
read moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
read morePREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Reports to Director of Clinical Trials or Clinical Research Nurse ...
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...
read moreInteracts with Research Sponsors, site personnel, IRBs (Institutional Review Boards), and other research entities regarding Regulatory and research study-related issues. Understand, monitor, and repor...
read moreThe Clinical Research Coordinator will be responsible for coordinating clinical research activities within the research division through the use of Good Clinical Practice Guidelines. PREFER: Certified...
read moreThe Clinical Research Coordinator will be responsible for coordinating clinical research activities within the research division through the use of Good Clinical Practice Guidelines. PREFER: Certified...
read morePREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Reports to Director of Clinical Trials or Clinical Research Nurse ...
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