Clinical Research Coordinator

Job overview

The Clinical Research Coordinator role is onsite in Puerto Rico; the listing identifies the location as 00901. The schedule is Monday through Friday, 7:00 a.m.–4:00 p.m. Pay is $20–$23 per hour. The coordinator supports clinical studies and participant safety while helping protect research data integrity. The coordinator manages day-to-day study operations from planning and enrollment through documentation and closeout. The role keeps protocols on track, supports participants, monitors safety and compliance, and coordinates study records, specimens, supplies, and staff training.

What you'll do

• Coordinate study projects and protocol events
• evaluate clinical data
• monitor compliance with protocols and regulations
• screen and enroll participants and document informed consent
• oversee participant care during visits
• record and report adverse events
• maintain study and regulatory records
• prepare study materials and reports
• review protocols and identify issues
• support audits
• train staff
• collect and process specimens
• coordinate study supplies and logistics.

What we're looking for

Skills & competencies

clinical research coordinator

puerto rico

phasewell research

$20–$23 per hour

monday–friday

7:00 a.m.–4:00 p.m.

clinical studies

participant enrollment

informed consent

research compliance

spanish and english

study documentation

Work arrangement

• Weekend coverage required

Benefits & perks

• 100% employer-paid health insurance.

Why this role

Requires fluency in Spanish and English, a bachelor’s degree in life sciences or a related field, and 3–5 years of clinical research or related experience. Master’s degree preferred.

About the employer

PhaseWell Research is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.