Unique opportunity to make an Impact in the healthcare industryโฆย
Revival Research Institute, LLCย was established in 2015, andย headquarteredย in the Metro Detroit Region,ย and has been growing ever since.ย Revivalย now has a national presenceย inย theย Metro-Detroitย Region,ย Texas, Illinois,ย andย Arizona.ย We have beenย nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.ย ย
Asย Revival Researchย Instituteย is growing, we are looking to add moreย qualifiedย professionalsย to our team,ย who are looking for an opportunity to grow and learn with us.ย ย
We are seekingย aย full-timeย Clinical Research Coordinatorย with a minimum ofย 2ย yearย ofย clinicalย experience, for our Woman's Health site.ย Someone with a strongย interestย in theย Clinical Researchย fieldย would be an excellent fit for ourย entry levelย position, with room to grow.ย However,ย this interest and background is not necessary, as our idealย candidate is an individual who isย detail orientated,ย being able toย maintainย organized records, as well asย someone who isย motivated to learn new things, as our companyย is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.ย ย
Clinical Research Coordinatorsย here atย Revival Research Institute,ย should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Clinical Research Coordinatorsย are responsible to coordinate and manage multiple studies.ย They are alsoย responsible for assisting the Investigators along withย other clinical staff,ย withย anyย study related tasks as follows but not limited to:ย
Participates in research participant screening,ย recruitmentย 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,ย processingย and shipping of research specimens, where applicable.ย
Documentsย study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain,ย reviewย and maintain source documents.ย
Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods.ย
Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversightย e.g.ย study amendments, adverse event reporting, protocol deviation reporting.ย
Maintain professional and technical knowledge about Clinical trials.ย
Research participant/family communication, protect patient confidentiality.ย
Preferred Qualifications:ย
Education/ Training: Bachelor's degree in health-related field with one toย twoย years relevant clinical experience ORย Master'sย degree in medical related field with noย research experience.ย Individuals with moreย experience are preferred, if qualifications exceed entry level, higher positions available.ย
ย Phlebotomy skills preferred.ย
Certifications, Licensures, and Registrations: National Certification (CRA or ACRP),ย BLS Certification.ย ย
Additionalย 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, secretarialย staffย and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.ย
IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!ย
Powered by JazzHR
cL3L2ZOIaF