International Medical Graduate (IMG) - Clinical Research Coordinator
Revival Research Institute, LLC, Southfield, MI, United States
Overview
Unique opportunity to make an Impact in the healthcare industry…
Revival Research Institute, LLC was established in 2015, 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, and Arizona. 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.
Job Summary
We are seeking International Medical Graduates with a minimum of 3 years 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 oriented, 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.
Responsibilities
Coordinating and managing multiple studies.
Assisting the Principal Investigators and other clinical staff with any study related tasks.
Research participant screening, recruitment and enrollment.
Consent and conduct research visits for data collection
o risk trials or 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, handle data queries and participate 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.
Qualifications
International Medical Graduate.
Minimum of 3 years of research experience.
Detail oriented, organized records.
Motivated to learn new things.
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 preferred.
Phlebotomy skills 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
JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!!
#J-18808-Ljbffr
Unique opportunity to make an Impact in the healthcare industry…
Revival Research Institute, LLC was established in 2015, 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, and Arizona. 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.
Job Summary
We are seeking International Medical Graduates with a minimum of 3 years 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 oriented, 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.
Responsibilities
Coordinating and managing multiple studies.
Assisting the Principal Investigators and other clinical staff with any study related tasks.
Research participant screening, recruitment and enrollment.
Consent and conduct research visits for data collection
o risk trials or 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, handle data queries and participate 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.
Qualifications
International Medical Graduate.
Minimum of 3 years of research experience.
Detail oriented, organized records.
Motivated to learn new things.
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 preferred.
Phlebotomy skills 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
JOIN US & GROW YOUR KNOWLEDGE & EXPERIENCE!!!
#J-18808-Ljbffr