Clinical Trials Coordinator: Data-Driven Patient Research

Lifespan; Providence (RI); On-site; USD 64,480 - 106,412; Full time

Job summary

Lifespan is seeking a Clinical Research Coordinator in Providence, Rhode Island, responsible for assisting in patient interaction and data analysis for clinical research projects. The role includes coordinating participant follow-up, ensuring compliance with study protocols, and performing statistical analyses.

The ideal candidate has a BA/BS, relevant experience, excellent organizational and communication skills, and is comfortable working with older adult populations.

Qualifications

• 1-2 years of related experience in clinical research and administration.
• Experience with electronic medical records and nursing assessments.
• Strong skills in prioritization and knowledge of research methodology.

Responsibilities

• Assist Principal Investigators with clinical research activities.
• Coordinate data collection and ensure protocol adherence.
• Monitor and follow up on patient appointments and documentation.

Skills

Organizational skills

Communication skills

Phlebotomy and EKG skills

Interpersonal skills

Analytical skills

Proficiency in computer data entry

Education

BA/BS in a related field

Tools

Electronic medical records/Epic

Office suite

Zoom

Job description

Lifespan is seeking a Clinical Research Coordinator in Providence, Rhode Island, responsible for assisting in patient interaction and data analysis for clinical research projects. The role includes coordinating participant follow-up, ensuring compliance with study protocols, and performing statistical analyses.

The ideal candidate has a BA/BS, relevant experience, excellent organizational and communication skills, and is comfortable working with older adult populations.