Clinical Research Coordinator

Revival Research Institute, LLC•Cary, NC

1d•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