Clinical Research Assistant: Data, Patients & Protocols

Brown-University-Health-1; Providence (RI); On-site; USD 42,000 - 69,000; Full time

Job summary

Brown University Health is seeking a Clinical Research Assistant to support multiple studies. You will recruit, collect, and analyze patient information, interview participants, and maintain study records.

Data entry and basic statistical analyses will be performed using computer software, with opportunities to contribute to study manuscripts. Under supervision, you will help develop protocols, review literature, and ensure informed consent is obtained.

Qualifications

• Bachelor's Degree in Applied or Life Sciences with research methodologies coursework.
• 3–6 months on-the-job experience with research studies.
• Knowledge of research methodology theory and data handling.
• Ability to organize multiple projects and prepare records and reports.
• Interpersonal abilities to interact with patients, families, and hospital staff.
• Analytical skills for developing protocols and statistical analyses.
• Technical ability to operate and maintain computer systems.
• Understanding patient care across aging processes and cultural patterns.

Responsibilities

• Coordinate clinical research activities with investigators and studies.
• Identify and follow up with patients meeting inclusion criteria; obtain consent.
• Maintain study records; interview patients/families and collect data.
• Enter data into databases and perform basic statistical analyses; generate graphs.

Skills

Interpersonal skills

Analytical skills

Organizational skills

Technical ability

Geriatric care awareness

Data entry

Education

Bachelor's Degree in Applied or Life Sciences

Job description

Brown University Health is seeking a Clinical Research Assistant to support multiple studies. You will recruit, collect, and analyze patient information, interview participants, and maintain study records.

Data entry and basic statistical analyses will be performed using computer software, with opportunities to contribute to study manuscripts. Under supervision, you will help develop protocols, review literature, and ensure informed consent is obtained.