Revival Research Institute, LLC·Cary, North Carolina
The Clinical Research Coordinator manages multiple clinical studies, including participant recruitment, screening, and enrollment. They are also responsible for collecting and processing research specimens, maintaining trial documentation, and ensuring compliance with regulatory standards.
Unique opportunity to make an Impact in the healthcare industry…
Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.
As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.
We are seeking a full-time Clinical Research Coordinator with a minimum of 2 year of clinical experience, for our Woman's Health site. Someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.
Clinical Research Coordinators here at Revival Research Institute, should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. They are also responsible for assisting the Investigators along with other clinical staff, with any study related tasks as follows but not limited to:
1. 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.
2. 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.
3. Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods.
4. 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.
5. Maintain professional and technical knowledge about Clinical trials.
6. Research participant/family communication, protect patient confidentiality.
Bachelor's degree in health-related field with one to two years relevant clinical experience OR Master's degree in medical related field with no research experience. Individuals with more experience are preferred, if qualifications exceed entry level, higher positions available.
2. Phlebotomy skills preferred.
National Certification (CRA or ACRP), BLS Certification.
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.
Improve the future as our clinical research coordinator!!!
Candidates must have a minimum of two years of clinical experience and a bachelor's degree in a health-related field, or a master's degree in a medical field. Proficiency in Microsoft Office, strong organizational skills, and knowledge of FDA regulations and Good Clinical Practices are required.
Market context
Clinical Research Coordinator roles in North Carolina are often in steady demand at hospitals, universities, and research sites that support ongoing studies. Competition tends to center on candidates who pair a related bachelor’s degree with hands-on clinical research or medical setting experience, plus familiarity with GCP/ICH rules, medical terminology, and procedures like phlebotomy. If you are considering applying, compare the posted requirements and benefits carefully; on this platform, they are AI-summarized from the original job description to save you research time.
Phlebotomist/Lab Tech
Phlebotomist/Lab Tech
International Medical Graduate (IMG) - Clinical Research Coordinator