Clinical Research Coordinator - Endocrinology
Listed on 2025-12-02
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Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Unique opportunity to make an Impact in the healthcare industry…
Revival Research Institute, LLCwas established in 2015, andheadquarteredin the Metro Detroit Region,and has been growing ever since.
Revivalnow has a national presenceintheMetro-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.
AsRevival Research Instituteis growing, we are looking to add morequalifiedprofessionalsto our team,who are looking for an opportunity to grow and learn with us.
We are seekingafull-timeClinical Research Coordinatorwith a minimum of2-3 yearofclinicalexperience, Ideally would also have Endocrinology experience.
Additionally,someone with a stronginterestin the Clinical Researchfieldwould be an excellent fit for our position, with room to grow. Our ideal candidate is an individual who isdetail orientated,being able tomaintainorganized records, as well assomeone who is motivated to learn new things, as our companyis 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 Coordinatorshere atRevival 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 withother clinical staff,withanystudy 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.
Documentsstudy related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain,reviewand 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 oversighte.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:
Education/ Training:
Bachelor's degree in health-related field with one totwoyears relevant clinical experience ORMaster'sdegree in medical related field with noresearch experience.
Individuals with mo reexperience are preferred, if qualifications exceed entry level, higher positions available.
Phlebotomy skills preferred.
Certifications, Licensures, and Registrations:
National Certification (CRA or ACRP),BLS Certification.
Additional Qualifications:
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, secretarialstaffand ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.
IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!
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