Clinical Research Coordinator

About the role

Revival Research Institute, LLC is a healthcare-focused company established in 2015, headquartered in the Metro Detroit region. With a growing national presence in Metro-Detroit, Texas, Illinois, and Arizona, Revival is known for providing high-quality data for clinical research trials.

Responsibilities

• Participates in research participant screening, recruitment, and enrollment.
• Consents and conducts research visits for data collection/no risk trials or no study article/minimal risk trials with oversight.
• Collects, processes, and ships research specimens, where applicable.
• Documents study related information in case report forms or electronic data capture systems, handles data queries, and participates in monitoring visits.
• Obtains, reviews, and maintains source documents.
• Maintains organization of all trial related documents and correspondence.
• Implements quality control and assurance methods.
• Communicates with study sponsors, research team, and the Institutional Review Board.
• Aids in the preparation of basic regulatory documents, such as study amendments, adverse event reporting, and protocol deviation reporting.
• Maintains professional and technical knowledge about clinical trials.
• Communicates with study participants and families, ensuring patient confidentiality.

Requirements

• Minimum 2 years of clinical experience.
• Bachelor's degree in health-related field or Master's degree in medical related field with relevant clinical experience.
• Phlebotomy skills preferred.
• National Certification (CRA or ACRP) and BLS Certification.
• Expertise in database and computer skills: Microsoft Office (Word, Excel), Outlook.
• Excellent verbal and written communication skills.
• Ability to work independently and assume responsibility.
• Strong organizational skills.
• Ability to meet data deadlines and maintain confidentiality.
• Knowledge of FDA Regulations and Good Clinical Practices.

Qualifications

• Education/Training: Bachelor's degree in health-related field with 2 years of relevant clinical experience OR Master's degree in medical related field with no research experience.
• Experience: Higher positions available for those with more experience.

Skills

• Detail-oriented.
• Organized record-keeping.
• Motivated to learn and grow.

Benefits

Not specified.

Pay

Not specified.

Schedule

Not specified.