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Clinical Trials Clinical Coordinator Jobs in North Carolina

Currently, there are no Clinical Trials Clinical Coordinator jobs available in North Carolina which match this search. You may wish to explore similar job titles on the Administrative jobs in North Carolina page or view related jobs below.
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Occupational Summary: The Clinical Trials Coordinator II (CTC II) develops, coordinates and implements the management of the clinical endpoint adjudication process for clinical trials research conducted by Principal Investigator(s) at Duke Clinical Research Institute (DCRI). The CTC II also performs a variety of duties involved in the organization, oversight, documentation and compilation of clin...
Position Title CLINICAL TRIALS COORDINATOR I - DCRI Clinical Events & Safety Requisition Number 401050284 Auto req ID 75141BR Location Durham Duke Entity MEDICAL CENTER Department Name DCRI - Clinical Events Commitee Shift First/Day Full Time / Part Time FULL TIME Job Code 1941 CLINICAL TRIALS COORDINATOR I Job Family Level 79 Job Description Occupational Summary: The CEC CTC is respon...
Position Title CLINICAL TRIALS COORDINATOR II - DCRI Clinical Events & Safety Requisition Number 401043807 Auto req ID 74685BR Location Durham Duke Entity MEDICAL CENTER Department Name DCRI - Clinical Events Commitee Shift First/Day Full Time / Part Time FULL TIME Job Code 1944 CLINICAL TRIALS COORDINATOR II Job Family Level 80 Job Description Minimum Qualifications Duke University is ...
Highly preferred experience: - Experience managing large, international commercial trials - Experience working cross-functionally with various departments - Direct management experience Occupational Summary Develop, coordinate, and implement research and administrative strategies essential to the successful management of phase II, III and/or IV clinical trials research projects conducted by p...
Clinical Research Careers at an Innovative Site Specific Research Organization (SSRO) CTMG Inc. is interviewing LPNs, CMAs, and RMAs who want the opportunity to achieve greatness! The successful candidate will enjoy a fast-paced work environment, be skilled in multi-tasking and problem-solving, and contribute ideas for consideration by the team as together we change how clinical trials are manage...
Clinical Research Careers at an Innovative Site Specific Research Organization (SSRO) CTMG Inc. is interviewing RNs and PAs who want the opportunity to achieve greatness! The successful candidate will enjoy a fast-paced work environment, be skilled in multi-tasking and problem-solving, and contribute ideas for consideration by the team as together we change how clinical trials are managed to buil...
Occupational Summary: As the world’s largest academic clinical research organization, the Duke Clinical Research Institute (DCRI) offers many unique career opportunities in a variety of fields. Currently, DCRI has opportunities for Clinical Trials Project Leaders with experience in full life cycle clinical trials project management, Phase II-IV multi-center research projects, managing multiple pr...
OCCUPATIONAL SUMMARY Working in a matrix management environment, serve as an expert resource to project team members to oversee and facilitate the development and implementation of tools, plans and strategies for managing sites and clinical monitoring activities for clinical research projects in assigned Therapeutic Area(s) (TA). Serve as supervisor for assigned Clinical Operations staff within a...
Occupational Summary Imagine a truly collaborative atmosphere. One where diverse research professionals work side-by-side with expert faculty and world renowned researchers. One where publication opportunities abound. One where your colleagues are mission-driven and keen on sharing data and knowledge with each other, and the world at large. As the world’s largest academic clinical research organ...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Clinical Project Manager- Work from home, anywhere in the US Apply Raleigh, NC Full-Time $95,000 - $150,000 Job Details If you are a Clinical Project Manager with Early Phase oncology experience, please read on! This is a work from home position. You can be located anywhere in the US. Offering full time W...
Position Title CLINICAL TRIALS ASSISTANT II - DCRI Clinical Operations Requisition Number 401014654 Auto req ID 72508BR Location Durham Duke Entity MEDICAL CENTER Department Name DCRI - Site Support & Management Shift First/Day Full Time / Part Time FULL TIME Job Code 52 CLINICAL TRIALS ASSISTANT II Job Family Level 08 Job Description Ideal candidates will possess experience tracking, co...
Perform independent and dependable work in preparation and coordination of study submission to IRB and other appropriate committees following regular deadlines. They will provide draft IRB, Sponsor and other response to the PI for approval. They will respond on behalf of the PI when appropriate Communicate with study staff, IRB, sponsors, domestic and international study partners in a courteous a...
The Clinical Research Coordinator selected for this role will work independently at Unified Women's Clinical Research's newest location based out of a busy Morehead City OB/GYN office setting, under the supervision of the central UWCR office based in Winston-Salem NC. Relocation package options available as applicable. Job Responsibilities Include the Following: Recruit research participants thr...
OCCUPATIONAL SUMMARY This position is with the Wake County Research team at Duke Raleigh assisting in the coordination of clinical research trials for the Duke Cancer Institute's (DCI) Oncology Clinical Research Unit (OncCRU). W ORK PERFORMED Organize and assist with maintenance of study documents and binders. Develop and maintain database(s) to track and monitor data collection. Build and ma...
The CTA II position for clinical research is an integral part of conducting all research-related tasks. The position is responsible for collecting data from study enrolled patients in both industry trials and federally supported research trials such as the National Institute of Health and Aging. The CTA II position assists the research coordinator in collecting data from patients in the pre-oper...
Position Title CLINICAL TRIALS SPECIALIST Requisition Number 401068987 Auto req ID 76474BR Location Durham Duke Entity MEDICAL CENTER Department Name DCI OFFICE OF RESEARCH SUPPORT Shift First/Day Full Time / Part Time FULL TIME Job Code 70 CLINICAL TRIALS SPECIALIST Job Family Level 10 Job Description OCCUPATIONAL SUMMARY This position is with the Wake County Research team at Duke Rale...
Position Title CLINICAL TRIALS ASSISTANT II Requisition Number 401067077 Auto req ID 76392BR Location Durham Duke Entity MEDICAL CENTER Department Name Medicine-Pulmonary Shift First/Day Full Time / Part Time FULL TIME Job Code 52 CLINICAL TRIALS ASSISTANT II Job Family Level 08 Job Description Work Performed Perform a variety of research, data base and clerical duties of a complex and ...
This position will develop, coordinate, and implement research and administrative strategies essential to the successful management of clinical trials research projects conducted by principal investigator(s) at Duke Clinical Research Institute (DCRI); perform avariety of duties involved inthe organization, documentation,compilation,and reporting of clinical research data. Project Management Reco...
Occupational Summary Coordinate and perform a variety of research and administrative activities required in the management of clinical trials research, as defined in DOCR RMT agreements with DUMC investigators at Duke and the Durham VA Hospital. Work Performed Perform specific project tasks per RMT agreements with individual investigators and study teams which may include but are not limited to...
Work Performed Perform a variety of research, data base and clerical duties of a complex and technical nature in support of multi-center clinical trials to assist investigators in organizing, gathering and compiling clinical research data. Maintain and update site demographics on computer data base; log forms received and file as appropriate; prepare reports from data base to include weekly repo...