See all roles

International Medical Graduate (IMG) - Clinical Research

Work from home Full-time role Hiring

Job Description

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, 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. 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 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!!! 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: 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
  • Knowledge of FDA Regulations and Good Clinical Practices

Apply tot his job Apply To this Job

You might like

Site Enablement Specialist

Work from home Full-time role

Data Analyst (Data Governance)

Work from home Full-time role

Remote Data Entry Specialist – Precision Data Management, Remote‑First Role, $30/hr – Join arenaflex’s Growing Virtual Team

Work from home Full-time role

Remote Data Entry Specialist – Precise Database Management, Confidential Records Handling & Team Collaboration

Work from home Full-time role

Remote Data Entry Specialist – Home‑Based Accurate Information Management & Team Collaboration at arenaflex

Work from home Full-time role

[Remote] Data Management Associate at Systems Thinking & Solutions

Work from home Full-time role

Chemistry Research Experts (PhDs)

Work from home Full-time role

Medicinal Chemist

Work from home Full-time role

Computational Chemist

Work from home Full-time role

Chemistry - Graduates - AI Training - Seattle, US

Work from home Full-time role

Experienced Data Entry Specialist – Flexible Remote Opportunity with arenaflex

Work from home Full-time role

Experienced Remote Data Entry Specialist – Flexible Work Arrangements at arenaflex

Work from home Full-time role

Experienced Data Entry Assistant – Entry Level Position at arenaflex

Work from home Full-time role

Design Consultant

Work from home Full-time role

Customer Service Supply Chain Specialist – arenaflex Chicago (Remote)

Work from home Full-time role

Experienced Data Entry Associate – Entry-Level Opportunity to Kickstart Your Career at arenaflex

Work from home Full-time role

[Remote] Global Account Manager, Telco

Work from home Full-time role

U.S. Licensing Specialist

Work from home Full-time role

Experienced Data Entry Specialist – Remote, Entry-Level Opportunity at arenaflex

Work from home Full-time role

Experienced Data Entry & Mail Room Clerk – Draper, UT

Work from home Full-time role