Clinical Research Coordinator
Revival Research Institute, LLC • Cary, NC60d • Onsite
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Clinical Research Coordinator
Revival Research Institute, LLC•Cary, NC
•Onsite
About The Position
Revival Research Institute, LLC, established in 2015 and headquartered in the Metro Detroit Region, has expanded nationally to Texas, Illinois, and Arizona. The institute is recognized for providing high-quality data for its clinical research trials. As the company grows, it is seeking qualified professionals to join its team. This full-time Clinical Research Coordinator position is for the Woman's Health site. While a minimum of 2 years of clinical experience is preferred, individuals with a strong interest in clinical research and a detail-oriented, organized, and motivated approach to learning new things are encouraged to apply, as the company expands into new therapeutic areas. The role emphasizes respect for diverse points-of-view and fostering an inclusive environment.
Requirements
- minimum of 2 year of clinical experience
- strong interest in the Clinical Research field
- detail orientated
- being able to maintain organized records
- motivated to learn new things
- Expert database and computer skills: Microsoft Office (Word, Excel), Outlook
- excellent verbal and written communication skills
- ability to work independently and assume responsibility
- excellent organizational skills
- ability to meet data deadlines and maintain confidentiality
- Maintain data integrity within the department
- Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff
- Knowledge of FDA Regulations and Good Clinical Practices
Nice To Haves
- Bachelor's degree in health-related field with one to two years relevant clinical experience
- Master's degree in medical related field with no research experience
- Phlebotomy skills
- National Certification (CRA or ACRP)
- BLS Certification
Responsibilities
- Participates in research participant screening, recruitment and enrollment
- Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight
- Responsible for collecting, processing and shipping of research specimens, where applicable
- Documents study related information in case report forms or electronic data capture systems
- handles data queries and participates in monitoring visits
- Obtain, review and maintain source documents
- Maintains organization of all trial related documents and correspondence
- Implement quality control and assurance methods
- Communicate with study sponsors, research team and the Institutional Review Board
- Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting
- Maintain professional and technical knowledge about Clinical trials
- Research participant/family communication, protect patient confidentiality
- coordinate and manage multiple studies
- assisting the Investigators along with other clinical staff, with any study related tasks
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
Number of Employees
11-50 employees
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