Job Description
Unique opportunity to make an Impact in the healthcare industry… Revival Research Institute, LLC was established in 2015, andheadquarteredin the Metro Detroit Region,and has been growing ever since.Revivalnow has a national presenceinthe
Metro-DetroitRegion,Texas, Illinois,andArizona. We have beennationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.
As
Revival ResearchInstitute is growing, we are looking to add morequalifiedprofessionalsto our team,who are looking for an opportunity to grow and learn with us.
We are seekingafull-time
Clinical Research Coordinator with a minimum of2-3 yearofclinicalexperience, Ideally would also have Psychiatric experience.Additionally,someone with a stronginterestin theClinical Researchfieldwould be an excellent fit for our position, with room to grow. Our idealcandidate is an individual who isdetail orientated,being able tomaintainorganized records, as well assomeone who ismotivated 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 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 Coordinatorsare responsible to coordinate and manage multiple studies.They are alsoresponsible for assisting the Investigators along withother clinical staff,withanystudy related tasks as follows but not limited to:
- Participates in research participant screening,recruitmentand enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting,processingand 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 moreexperience are preferred, if qualifications exceed entry level, higher positions available
- Phlebotomy skills preferred
- Certifications, Licensures, and Registrations: National Certification (CRA or ACRP),BLS Certification
- AdditionalQualifications: 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
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