The Clinical Epidemiology Division at the Barbara Davis Center (BDC) has a robust clinical research program designed to improve health conditions in adults living with Type 1 Diabetes. One (1) year clinical research or related clinical or data management experience. Two (2) years clinical research o...
A company is looking for a Clinical Research Physician to provide medical and scientific leadership in clinical trials. ...
Under the supervision of the Clinical Research Manager/ PI, the primary responsibility of the Professional Research Assistant is to serve as the clinical research coordinator in support of various research activities within Dr. This is a position requiring interest in medical research, the ability t...
Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
Clinical Science Professionals perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e....
They currently have 18 clinical research sites - half of them are embedded into physician offices and the other half are stand-alone sites 100% dedicated to research. Amazing opportunity for an experienced Lead Clinical Research Coordinator or a SR CRC with leadership experience to move into a Manag...
Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e. Job Title: Research Services Clinical Science Professional (Open Rank). Obtain study subject's medical history and current medication information, reviews resear...
Clinical Science Professionals perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e....
With world-class health sciences research, educational and clinical facilities, the CU School of Medicine has established distinctive and highly productive programs, receiving research awards of more than $350 million per year, including more than $200 million from National Institutes of Health and ...
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) preferred. Experience with overseeing work at clinical sites and contract research organizations (pre-clinical and clinical). Currently, we have an opening for a Clinical Research Coordinator in our Lou...
Contact appropriate individuals (, study site staff or study site Clinical Research Associate) regarding incomplete, inaccurate, or missing photos, acetate tracings, and other Endpoint and Specialty Services Core Lab documents as required by the project. Thorough knowledge of the Good Clinical Pract...
FTE) Clinical Research Coordinators (Research Services Clinical Science Professionals). Candidates in this role will be integrated into the clinical trials arm of the Psychiatry Research Innovations unit (PRI), which is a research support center within the Department of Psychiatry that provides rese...
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e. Research Services Clinical Science Professional-34155University Staff. Job Title:Research Services Clinical Science Professional. The BDC also serves as a clinic...
Senior Clinical Trial Manager leads and serves as the primary point of contact for clinical trials site operations. Serve as the secondary contact to address site questions, when the site Clinical Research Associate (CRA) is unavailable. A minimum of years of experience in clinical research setting...
Senior Clinical Research Coordinator. Coordinator who can work across multiple complex modalities and is responsible for participating in the day-to-day operations of complex, multi-site clinical research programs and/or studies conducted by Principal Investigators (PIs) at the University of Colorad...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
A minimum of years of experience in a clinical research setting or year of experience at CPC as Research Assistant is required. Do you have clinical research background? Are you open to travel of up to % of the time? Do you adapt to change easily? Can you quickly connect and build strong relations...
Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN to support our Aurora and Centennial locations. Responsible for education of clinic staff regarding clinical research. Expe...
Contact appropriate individuals (, study site staff or study site Clinical Research Associate) regarding incomplete, inaccurate, or missing photos, acetate tracings, and other Endpoint and Specialty Services Core Lab documents as required by the project. Thorough knowledge of the Good Clinical Pract...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
The Clinical Product Regulatory Specialist is responsible for management of regulatory and investigational product (IP/IMP) activities to support CPC’s clinical trials. We are looking for a Clinical Product Regulatory Specialist to join our team!. Prepare regulatory document templates for distributi...
Serve as the secondary contact to address site questions when the site Clinical Research Associate (CRA) or Research Assistant (RA) is unavailable. Clinical Trial Manager II serves as the primary point of contact for clinical trials site operations. A minimum of years of experience in clinical rese...
CRO clinical research project/clinical operations management experience. Oversee clinical operations management activities when delegated to a Clinical Trial Manager (CTM). Review and finalize monitoring visit reports and follow-up letters with Clinical Research Associates (CRAs). Thorough knowledge...