Clinical Research Data Intern | Trials & Analysis

Tranquil Clinical Research and Consulting Services; Webster (TX); On-site; USD 28,000 - 36,000; Full time

Job summary

Tranquil Clinical Research and Consulting Services in Webster, TX seeks a Research Intern to support clinical trials by collecting, aggregating, and analyzing data, performing data entry, and handling clerical tasks under supervision.

The role emphasizes adherence to responsible conduct of research, basic data management, and study coordination, with training such as CITI required; a Bachelor’s degree may be required for some programs.

Qualifications

• Must adhere to the standards for the responsible conduct of research.
• Organizational skills and basic math, data collection and analysis, and research principles.
• Knowledge of human subjects research.
• Proficient in Windows and/or Mac; strong writing, editing and proofreading skills.

Responsibilities

• Maintain confidentiality of data and manage research projects.
• Ensure compliance with program guidelines and funding/regulatory requirements.
• Accurately complete IRB submissions on time.
• Collect data to facilitate operational and clinical research activities.
• Enter data into databases and sample tracking systems.
• Attend and contribute to team meetings; pursue required training and certifications.

Skills

Data entry

Research data analysis

Editing and writing

Windows/Mac proficiency

Attention to detail

CITI Certification

Education

High School Diploma or GED

Bachelor's Degree may be required

Job description

Tranquil Clinical Research and Consulting Services in Webster, TX seeks a Research Intern to support clinical trials by collecting, aggregating, and analyzing data, performing data entry, and handling clerical tasks under supervision.

The role emphasizes adherence to responsible conduct of research, basic data management, and study coordination, with training such as CITI required; a Bachelor’s degree may be required for some programs.