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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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Working from one of our office locations in Durham, NC, Billerica, MA of San Diego, CA as a Clinical Trial Specialist (CTS) you will conduct and facilitate specific start-up activities that may include site identification, feasibilities, essential document collection and review, ICF customization, EC submissions, preparation and negotiation of Clinical Site Contracts for site locations throughout ...
Job Req ID: 101912 Position Number: 00110680 Employment Type: Full Time Shift: Day Shift Details: Standard business hours Standard Hours:?40.00 Department Name: LCI Clinical Trials Location: Carolinas Medical Center Location Details:? Morehead ? ? ? Job Summary Coordinates the clinical, regulatory, business, and other research- related activities and documentation for clinical trials ...
Responsible for the successful planning, implementation and execution of contracted clinical monitoring activities. Functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial. Assures clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by Novella Clinical and ...
Novella Clinical is seeking a Home-based Clinical Trial Manager with Medical device experience. Responsible for the successful planning, implementation and execution of contracted clinical monitoring activities. Functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial. Assures clear client and internal team communication, process documentati...
Novella Clinical Resourcing is seeking a Clinical Trial Project Leader II - Clinical Events and Safety Surveillance: 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 principal investigator(s) at XXXX; perform a variety of duties involve...
Occupational Summary Develop, coordinate and implement research and administrative strategies essential to the successful management of clinical registry research conducted by principal investigator(s) in the Outcomes group at the DCRI; perform a variety of duties involved in the organization, oversight, documentation and compilation of clinical research data, including, but not limited to, writin...
This new Site Coordinator would join the DCRI Outcomes Research and Assessment Group to work on clinical registry projects. This individual would work closely with the Project Lead (PL) as a DCRI data liaison with participating STS sites. DCRI serves as data warehouse coordination and analysis center for multiple clinical registries, across the US. Typically, between 500 and 1000 sites participat...
Occupational Summary Develop, coordinate and implement research and administrative strategies essential to the successful management of pragmatic health systems research conducted by principal investigator(s) at Duke University Medical Center or within sponsored research networks; perform a variety of duties involved in the organization, oversight, documentation and compilation of health systems ...
Develop and implement research navigation programs and associated operational procedures of the MyResearchTeam@Duke Navigation Office. Facilitate the advancementof investigator-initiated clinical and translational research by linking investigators to relevant internal and external resources, tools and collaborators. Serve as the initial and main point of contact for investigator requests. ...
Overview With over 14,000 employees in 70 Countries, inVentiv Health offers best-in-class clinical development and commercialization services to global healthcare companies seeking to accelerate performance. Our people provide the brilliant ideas, valuable insight and relentless energy that drive biopharma products from lab to life. Here at inVentiv Health Selling Solutions, a critical segment o...
Occupational Summary: Coordinate and perform a variety of research and administrative activities required in the management of clinical trials research conducted by principal investigators at Duke University Medical Center; perform a variety of independent duties involved in the collection, documentation and compilation of clinical research data. Work Performed: Coordinate and perform a variety ...
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 principal investigator(s) at Duke University Medical Center; perform a variety of duties involved in the organization, documentation and compilation of clinical research data. Work Performed ...
Occupational Summary Coordinate and perform a variety of research and administrative activities required in the management of clinical trials research conducted by principal investigators at Duke University Medical Center; perform a variety of independent duties involved in the collection, documentation and compilation of clinical research data. Work Performed Coordinate and perform a variety of...
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 principal investigator(s) at Duke University Medical Center; perform a variety of duties involved in the organization, documentation and compilation of clinical research data; function in pre...
Occ Summary Perform a variety of research, data base and clerical duties of a complex and technical nature in support of multi-center clinical trials to ensure adherence to protocols and quality of information received. 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 ...
# Ensure that charges associated with grants and clinical trials are billed appropriately for both physician and hospital services. # Diligently work reports and work queues to decrease bill hold accounts, and assist in communicating trends to reduce customer service issues/service now request # Assist in educating principal investigators-study teams regarding compliance with government regulati...
Occ Summary Perform a variety of research, data base and clerical duties of acomplex and technical nature in support of multi-center clinical trials to ensure adherence to protocols and quality of information received. 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 i...
Position Title CLINICAL TRIALS SPECIALIST Requisition Number 401098194 Auto req ID 79056BR Location Durham Duke Entity MEDICAL CENTER Department Name Child & Fam Mental Health & Dev Neuro Shift First/Day Full Time / Part Time FULL TIME Job Description Clinical Trials Specialist Occupational Summary: Coordinate and perform a variety of research and administrative activities required in th...
Position Title CLINICAL TRIALS SPECIALIST Requisition Number 401107056 Auto req ID 79602BR Location Durham Duke Entity MEDICAL CENTER Department Name Behavioral Medicine Shift First/Day Full Time / Part Time FULL TIME Job Description Clinical Trials Specialist Occupational Summary: Coordinate and perform a variety of research and administrative activities required in the management of cl...
Job Description Regulatory Affairs, this position includes providing guidance and assistance to investigators and study teams who need FDA oversight for their research projects. This includes working on Initial Investigational New Drug or Investigational Device Exemption applications, requests for meetings with FDA and supporting documentation, and ensuring compliant maintenance of effective IND ...