Bilingual Clinical Research Lead - Study Operations

PhaseWell Research; San Juan (PR); On-site; USD 28,000 - 32,000; Full time

Benefits offered by this job

100% employer-paid health insurance

Job summary

PhaseWell Research is seeking an experienced bilingual Clinical Research Coordinator to lead our clinical studies from start to finish. You will coordinate day-to-day study operations, safeguard participant safety and data integrity, and keep protocols on track.

You will recruit and enroll participants, oversee informed consent, monitor safety, and manage study documentation. The role requires Spanish/English fluency, strong organizational skills, and experience with study technology.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 3–5 years in clinical research or related experience.
• Fluency in Spanish and English.
• Strong knowledge of biological and medical terminology.
• Excellent organizational and attention to detail.
• Excellent communication and interpersonal skills.
• Solid understanding of administrative and management principles.
• Comfort using study technology, including ePRO tablets and other electronic devices.

Responsibilities

• Lead study execution: plan, coordinate, and evaluate clinical research projects.
• Ensure protocol compliance with regulations and policies.
• Screen and enroll participants with informed consent oversight.
• Monitor participant care and enrollment status at study visits.
• Record adverse events and report to investigators and oversight bodies.
• Maintain study records, CRFs, drug dispensation, and regulatory docs.
• Prepare study materials, reports, and progress updates.
• Review and revise protocols for data management and risks.

Skills

Bilingual Spanish/English

Organizational skills

Communication skills

Interpersonal skills

Education

Bachelor’s degree in life sciences

Master’s degree preferred

Tools

ePRO tablets

EDC systems

Job description

PhaseWell Research is seeking an experienced bilingual Clinical Research Coordinator to lead our clinical studies from start to finish. You will coordinate day-to-day study operations, safeguard participant safety and data integrity, and keep protocols on track.

You will recruit and enroll participants, oversee informed consent, monitor safety, and manage study documentation. The role requires Spanish/English fluency, strong organizational skills, and experience with study technology.