Clinical Research Coordinator

Clinical Research Coordinator – Phase I

Location: Miami, FL – Full-Time, Onsite

Compensation: $30–$35/hour

The Opportunity

A leading clinical research organization is seeking an experienced Clinical Research Coordinator (CRC) to join a well-established Phase I clinical research site in Miami, Florida .

This is an excellent opportunity for a CRC with Phase I clinical trial experience who enjoys working in a fast-paced, highly protocol-driven research environment. The site conducts early-phase clinical trials involving healthy volunteers as well as selected patient populations , providing exposure to an important stage of the drug development process.

Candidates outside of the Miami area are encouraged to apply, as relocation assistance and a sign-on bonus may be available .

Key Responsibilities

As a Clinical Research Coordinator, you will be responsible for the day-to-day coordination and execution of assigned clinical trials while working closely with Principal Investigators, site leadership, sponsors, and study participants.

Responsibilities include:

• Coordinate assigned clinical trials in accordance with study protocols, GCP, ICH guidelines, FDA regulations, and site SOPs
• Develop a thorough understanding of assigned study protocols and study-specific requirements
• Support study start-up activities, including reviewing protocols and preparing source documentation
• Screen and enroll potential study participants
• Conduct and document the informed consent process with prospective participants
• Schedule and coordinate study visits and protocol-required procedures
• Perform study-related activities as delegated by the Principal Investigator
• Maintain accurate, complete, and organized study documentation
• Enter study data into paper and electronic data capture systems
• Communicate with sponsors, laboratories, IRBs, and other regulatory organizations as appropriate
• Work closely with investigators and site leadership to ensure protocol compliance and participant safety
• Identify, document, and escalate protocol deviations or violations as required
• Accurately document and track adverse events in accordance with study protocols
• Support participant recruitment and enrollment initiatives
• Attend Investigator Meetings when required
• Assist with study close-out activities and appropriate storage of study records
• Contribute to SOP development and process improvements as needed

Qualifications

Required:

• Previous Phase I clinical trial experience
• Bilingual in Spanish and English
• Understanding of Good Clinical Practice (GCP), ICH guidelines, and clinical research regulatory requirements
• Strong understanding of clinical trial coordination and study documentation
• Excellent written, verbal, and interpersonal communication skills
• Ability to work independently while collaborating effectively with investigators, sponsors, study participants, and site teams
• Strong organizational skills and attention to detail
• Comfortable working in a fast-paced, protocol-driven clinical research environment
• Basic proficiency with Microsoft Word and Excel and familiarity with clinical research systems/EDC platforms

Education:

• High school diploma or equivalent required
• College degree preferred

Why Consider This Opportunity?

This position offers the opportunity to work at an established early-phase clinical research site with significant exposure to Phase I drug development. The environment provides hands-on experience with complex protocols and direct involvement in study execution and participant care.

The organization offers:

• $30–$35/hour
• Medical insurance
• Dental and vision insurance
• 401(k) with employer matching
• Paid time off
• Opportunities for professional growth within clinical research

Schedule: Full-Time, Onsite – Miami, FL