Clinical Research Coordinator II: Trials & Compliance

University of Miami; Miami (FL); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Tuition remission

Job summary

University of Miami (UHealth) seeks a full-time Clinical Research Coordinator 2 to support clinical studies on the UHealth campus. The role involves planning, coordinating, implementing, monitoring and evaluating study activities according to sponsor and regulatory guidelines.

Responsibilities include participant recruitment, data collection, specimen handling, documentation, and communication with sponsor and study sites.

Qualifications

• Bachelor’s degree required; minimum 2 years of relevant experience.
• Ability to learn new procedures, technologies, and protocols and adapt to changing priorities.
• Strong written and verbal communication for interactions with colleagues and stakeholders.

Responsibilities

• Assists in participant recruitment and retention activities and screening for eligibility.
• Performs study procedures, data collection, and daily operations of moderate risk protocols.
• Collects, processes, packs, and ships specimens per protocol and regulations.
• Maintains study binders and filings per protocol requirements and department policy.
• Distributes study materials according to credentials and PI directions.
• Monitors and reports adverse events and protocol deviations.
• Assists with protocol amendments under PI supervision.
• Supports orientation and training for research staff.
• Keeps investigators apprised of study progress and submits progress reports.

Skills

Learning Agility

Teamwork

Technical Proficiency

Communication

Education

Bachelor's degree

Job description

University of Miami (UHealth) seeks a full-time Clinical Research Coordinator 2 to support clinical studies on the UHealth campus. The role involves planning, coordinating, implementing, monitoring and evaluating study activities according to sponsor and regulatory guidelines.

Responsibilities include participant recruitment, data collection, specimen handling, documentation, and communication with sponsor and study sites.