Clinical Research Coordinator - Endocrinology experience

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 2-3 year of clinical experience, Ideally would also have Endocrinology experience. Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our  position, with room to grow.

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 :

• 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.  Preferred Qualifications :