Research Intern

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

Description

The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also perform other duties such as data entry, and administrative duties such as filing, record keeping, photocopying, and creating flyers/posters. The Research Intern will be supervised by a senior research staff member or principal investigator.

Qualifications

Minimum Education: High School Diploma or GED (Required) or Bachelor's Degree (May require a Bachelor’s degree based on the specific internship program).

Minimum Work Experience: 0-2 years related experience. 2 years experience working in a medical or scientific research setting preferred.

• Required Skills/Knowledge:
  • Demonstrates adherence with the standards for the responsible conduct of research.
  • Work requires organizational skills, knowledge of basic mathematical, data collection and analysis, and research principles.
  • Knowledge of human subjects research.
  • Excellent computer skills in a Windows and/or Mac environment.
  • Excellent writing, editing, and proofing skills.
• Required Licenses And Certifications:
  • CITI Certification (Required)
  • Valid Driver's license

Functional Accountabilities

Research Projects

• Maintain confidentiality of data, as required.
• Plan, conduct and manage research projects.
• Responsible for appropriate use of research funds and resources.

Project Administration

• Ensure compliance with program guidelines and requirements of funding and regulatory agencies.
• Stay informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.
• Accurately complete IRB submissions on time.
• Anticipate study needs and work to accomplish them in a timely manner.
• Seek assistance, when needed.

Data Collection

• Collect data in order to facilitate operational and clinical research activities.
• Enter clinical and research data and information into database, include electronic CRFs and sample tracking databases.
• Follow established guidelines in the collection of clinical data and/or administration of clinical studies.
• Support aggregation and analysis of study data, as directed by senior research staff.

Professional Development

• Attend and contribute to team meetings, including working to set and achieve project timelines and deliverables.
• Obtain training and certification as required by study protocol (e.g., CITI training).
• Comply with all annual job-related training requirements.