Job detail

International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC

#Outlook #Regulatory Compliance #Phlebotomy #Microsoft Office #FDA Regulations #Patient Confidentiality #Specimen Processing #Clinical Research

Quick overview

The Clinical Research Coordinator will manage multiple studies, including participant screening, recruitment, and enrollment. They are also responsible for collecting and processing research specimens, maintaining source documents, and assisting with regulatory document preparation.

Requirements summary

Candidates must be International Medical Graduates with at least one year of research experience. Proficiency in Microsoft Office and knowledge of FDA regulations and Good Clinical Practices are required.

postgraduate degreeCommunicationPhlebotomyMicrosoft OfficeOrganizational skillsGood Clinical PracticesData collectionSpecimen processingClinical researchData integrityFDA regulationsPatient recruitmentParticipant screeningCase report formsElectronic data captureRegulatory document preparation

Job description

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, New Jersey, and N Carolina.
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 International Medical Graduates with a minimum of 1 year of research experience.
Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow.
We are looking for individuals that want the opportunity to learn and grow with us.
New Staff should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results.
Some responsibilities will include coordinating and managing multiple studies.
They are also responsible for assisting the Principal Investigators and other clinical staff, with any study related tasks as follows but not limited to: 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.
Document 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.
Maintain 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 of Clinical trials and Standards of Care.

International Medical Graduate (IMG) - Clinical Research Coordinator

Quick overview

Requirements summary

Job description

Preferred Qualifications

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