Clinical Research Coordinator

Revival Research Institute, LLC; Houston (TX); On-site; USD 50,000 - 70,000; Full time

Job summary

Revival Research Institute, LLC is seeking a full-time Clinical Research Coordinator with at least 2 years of clinical research experience to join our expanding team in Houston, Texas. The role includes managing multiple research studies, ensuring confidentiality, and maintaining compliance with regulations. Candidates should possess strong organizational and communication skills, with a desire to grow in the clinical research field.

Qualifications

• Minimum of 2 years of clinical research experience required.
• Education in health-related fields preferred.
• National Certification (CRA or ACRP) is a plus.

Responsibilities

• Coordinating and managing multiple clinical studies.
• Screening and enrolling research participants.
• Documenting study-related information accurately.

Skills

Organizational Skills

Verbal Communication

Written Communication

Attention to Detail

Education

Bachelor's degree in a health-related field

Master's degree in a medical-related field

Tools

Microsoft Office: Word

Microsoft Office: Excel

Microsoft Office: Outlook

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, with a growing national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We are recognized nationally for our commitment to providing high-quality data for clinical research trials.

As Revival Research Institute expands, we are looking to add more qualified professionals to our team—individuals eager to grow and learn with us.

We are seeking a full-time Clinical Research Coordinator with a minimum of 2 years of clinical research experience. An individual with a strong interest in the clinical research field would be an excellent fit, with room for growth. Our ideal candidate is detail-oriented, organized, motivated to learn new skills, and interested in expanding into new therapeutic areas. We value candidates who want to learn and grow with us.

Clinical Research Coordinators at Revival Research Institute should respect diverse perspectives and foster an inclusive environment that drives productivity and results. Responsibilities include coordinating and managing multiple studies, assisting investigators and clinical staff with study-related tasks, such as:

1. Screening, recruiting, and enrolling research participants. Conducting research visits for data collection, including minimal risk or no-risk trials, under oversight. Responsible for collecting, processing, and shipping research specimens where applicable.

2. Documenting study-related information in case report forms or electronic data capture systems, handling data queries, and participating in monitoring visits. Obtaining, reviewing, and maintaining source documents.

3. Organizing trial-related documents and correspondence. Implementing quality control and assurance measures.

4. Communicating with study sponsors, research teams, and the Institutional Review Board. Assisting with regulatory document preparation, including study amendments, adverse event reporting, and protocol deviations.

5. Maintaining professional and technical knowledge about clinical trials.

6. Communicating with research participants and their families, ensuring patient confidentiality.

Preferred Qualifications:

1. Education/Training: Bachelor's degree in a health-related field with 1-2 years of relevant clinical experience, or a Master's degree in a medical-related field with no research experience. Candidates with more experience are preferred and may qualify for higher positions.

2. Phlebotomy skills are preferred.

3. Certifications: National Certification (CRA or ACRP), BLS Certification.

4. Additional skills: Proficiency in databases and computer skills (Microsoft Office: Word, Excel, Outlook), excellent verbal and written communication, ability to work independently and responsibly, strong organizational skills, ability to meet data deadlines, and maintain confidentiality. Knowledge of FDA regulations and Good Clinical Practices is required.

IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!