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Senior Clinical Research Coordinator - 249543
🏢 Medix™
Salary not disclosed
Senior Clinical Research Coordinator Opportunity in Miami, FL (33155)
Position Summary
The Clinical Research Coordinator plays an integral role in supporting the day-to-day operations of clinical trials at the investigator site. This position is responsible for planning, coordinating, and executing clinical studies in compliance with study protocols, contracted scope of work, ICH/GCP guidelines, sponsor and CRO requirements, and applicable local regulations.
Duties/Responsibilities
- Coordinate study startup activities, including site selection visits, source documentation setup, recruitment planning, and site preparation.
- Lead weekly site meetings and collaborate with site leadership to address facility and operational needs.
- Manage investigator signature processes and support subject recruitment, enrollment, and contingency planning.
- Monitor and track screening, enrollment, and study milestones, identifying barriers and implementing solutions.
- Partner with recruitment teams to improve enrollment for difficult-to-fill studies.
- Ensure timely and accurate data entry in EDC and clinical trial management systems, addressing discrepancies as needed.
- Participate in study initiation, monitoring, and close-out visits, including reviewing monitor reports and following up on action items.
- Conduct quality checks on subject visits and collaborate with compliance teams to address issues.
- Work with source documentation staff to ensure readiness for patient visits.
- Provide training, mentorship, and troubleshooting support to site staff; assist with onboarding new employees and evaluating training progress.
- Act as a liaison between site operations, financial teams, and leadership to improve workflows and communication.
- Develop and maintain strong investigator and sponsor relationships while providing progress updates.
- Participate in staff evaluations, candidate interviews, and employee development activities.
- Deliver presentations at training events and contribute to external collaborations for specialized study protocols.
- Support SOP development, special projects, business development initiatives, and team-building activities.
- Perform other duties as assigned.
Required Skills/Abilities
- Strong knowledge of medical terminology, ICH/GCP, and regulatory requirements.
- Excellent interpersonal, communication, and organizational skills.
- Proficiency with Microsoft Office, including Excel.
- Bilingual in English and Spanish, with strong written and verbal skills.
- Ability to work independently and collaboratively within a team.
- Strong problem-solving skills with the ability to maintain confidentiality and build effective working relationships.
Education/Experience
- Bachelor's Degree Required
- Minimum 4+ years of clinical research coordinator experience, preferably with industry-sponsored trials.
Additional Details
- Location: Miami, FL (33155)
- Position: Senior Clinical Research Coordinator
- Employment: ~6 month (1,040 Hours) contracted probationary period into direct hire / permanent position
- Hours: Monday-Friday; 8:30AM-5PM; Onsite 5 Days a Week
- Pay Range: $66,000-$89,000 Annual Salary (Dependent on background and years of experience)
- Requirements: 4+ Years of Clinical Research Coordinating Experience; Bachelor's Degree Required
Not Specified
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