Clinical Research Intern — Data & IRB Support

Tranquil Clinical Research and Consulting Services; Webster (TX); On-site; USD 30,000 - 45,000; Full time

Job summary

Tranquil Clinical Research and Consulting Services is seeking a Research Intern to support clinical trials by performing research, database, and clerical tasks. The intern will focus on collecting, aggregating, and analyzing clinical research data while assisting investigators with data management.

This role requires a High School Diploma or GED, and up to 2 years of related experience, with a preference for those with a background in medical research. CITI Certification and excellent computer skills are mandatory.

Qualifications

• Minimum 0-2 years related experience; 2 years in medical/scientific research preferred.
• Requires CITI Certification and a valid driver's license.

Responsibilities

• Perform research, database, and clerical duties for clinical trials.
• Collect, aggregate, and analyze clinical research data.
• Ensure compliance with regulatory guidelines and best practices.

Skills

Organizational skills

Data collection

Research principles

Computer skills

Writing and editing

Education

High School Diploma or GED

Bachelor's Degree (preferred)

Job description

Tranquil Clinical Research and Consulting Services is seeking a Research Intern to support clinical trials by performing research, database, and clerical tasks. The intern will focus on collecting, aggregating, and analyzing clinical research data while assisting investigators with data management.

This role requires a High School Diploma or GED, and up to 2 years of related experience, with a preference for those with a background in medical research. CITI Certification and excellent computer skills are mandatory.