International Medical Graduate (IMG) - Clinical Research Coordinator
Revival Research Institute, LLC, Mercerville-Hamilton Square, NJ, United States
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, New Jersey, andN Carolina. 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 seeking
International Medical Graduates with a minimum of 1 year of research experience.Additionally,someone with a stronginterestin theClinical Researchfieldwould be an excellent fit for ourentry levelposition, 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. Someresponsibilities will includecoordinatingand managingmultiple studies.They are alsoresponsible for assisting the Principal Investigators and other clinical staff,withanystudy related tasks as follows but not limited to:
Research participant screening,recruitmentand enrollment. Consent and conduct research visits for data collection
o risk trials or no study article/minimal risk trials with oversight. Responsible for collecting,processingand shipping of research specimens, where applicable.
Documentstudy related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain,reviewand maintain source documents.
Maintainorganization 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 ofClinical trials and Standards of Care.
Protect patient confidentiality.
Preferred Qualifications
Education/ Training: InternationalMedical 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
Phlebotomy skills are also preferred.
AdditionalQualifications: 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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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, New Jersey, andN Carolina. 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 seeking
International Medical Graduates with a minimum of 1 year of research experience.Additionally,someone with a stronginterestin theClinical Researchfieldwould be an excellent fit for ourentry levelposition, 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. Someresponsibilities will includecoordinatingand managingmultiple studies.They are alsoresponsible for assisting the Principal Investigators and other clinical staff,withanystudy related tasks as follows but not limited to:
Research participant screening,recruitmentand enrollment. Consent and conduct research visits for data collection
o risk trials or no study article/minimal risk trials with oversight. Responsible for collecting,processingand shipping of research specimens, where applicable.
Documentstudy related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain,reviewand maintain source documents.
Maintainorganization 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 ofClinical trials and Standards of Care.
Protect patient confidentiality.
Preferred Qualifications
Education/ Training: InternationalMedical 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
Phlebotomy skills are also preferred.
AdditionalQualifications: 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.
#J-18808-Ljbffr