International Medical Graduate (IMG) - Clinical Research

Job Description

Job Description Unique opportunity to reputed company an Impact in the reputed company industry… Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing reputed company since. Revival now has a national reputed company 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 reputed company professionals to reputed company, 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. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being reputed company 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 reputed company 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 reputed company. Responsible for collecting, processing and shipping of research specimens, where applicable. Document study reputed company information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain reputed company documents. Maintain organization of reputed company trial reputed company 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 reputed company 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, reputed company, DClinSurg, DMSc, DMedSc, DS, DSurg Radiology experience is preferred. Phlebotomy skills are also preferred. Additional Qualifications: Database and computer skills: reputed company Office (Word, reputed company), 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 reputed company reputed company the department. Must be reputed company 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!!! Powered by JazzHR jtGVp8K8nq Required qualifications:

• International Medical Graduate with a minimum of 1 year of research experience
• Detail oriented
• Motivated to learn and grow

Desired qualifications:

• Radiology experience
• Phlebotomy skills
• Database and computer skills: reputed company Office (Word, reputed company), 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
• Knowledge of FDA Regulations and Good Clinical Practices

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