International Medical Graduate; IMG; Clinical Research Coordinator

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.

Revival now has a national presenceinthe
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 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 3 year of research experience.

Additionally,someone with a stronginterestin the Clinical Researchfieldwould be an excellent fit for ourentry level position, with room to grow.

However,this interest and background is not necessary, as our ideal candidate is an individual who isdetail orientated,being able tomaintainorganized records, as well assomeone who is motivated 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.

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 includecoordinatingand managing multiple studies.

They are also responsible for assisting the Principal Investigators and other clinical staff,withanystudy 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,reviewand 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 oversighte.g.study amendments, adverse event reporting, protocol deviation reporting.

Maintain professional and technical knowledge of Clinical trials and Standards of Care.

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, secretarialstaffand ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.

JOIN US& GROW YOUR KNOWLEDGE & EXPERIENCE!!!