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Job detail

International Medical Graduate (IMG) - Clinical Research Coordinator

Revival Research Institute, LLC

Employer page

#Outlook #Quality Control #Phlebotomy #Microsoft Excel #Microsoft Word #FDA Regulations #Data Management #Radiology #Data Integrity #Specimen Handling #Informed Consent #Clinical Trials

Full Time On Site 2-5 yrsPosted 1 month agoCloses Jul 21

Location

Corinth, Texas

Quick overview

Coordinate and manage multiple clinical studies while assisting principal investigators with participant screening, recruitment, and enrollment. Maintain accurate study documentation, handle data queries, and ensure compliance with regulatory standards and quality control methods.

Requirements summary

Candidates must be International Medical Graduates (IMG) with at least 3 years of research experience. Proficiency in Microsoft Office, strong organizational skills, and knowledge of FDA regulations and Good Clinical Practices are required.

postgraduate degreePhlebotomyMicrosoft OfficeOrganizational skillsCommunication skillsPatient confidentialityRadiologyGood Clinical PracticesData collectionSpecimen processingClinical researchData integrityFDA regulationsParticipant recruitment

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, North Carolina, New Jersey .
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 3 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.
However, this interest and background is not necessary, as 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.
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.
Protect patient confidentiality.

Preferred Qualifications

Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg Radiology experience is preferred. Phlebotomy skills are also preferred. Additional Qualifications: 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, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices. JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!!