Clinical Research Coordinator clinical trials network of America - 3.1 Fort Lauderdale, FL Job Details Full-time $75,000 - $85,000 a year 21 hours ago Benefits Health insurance Dental insurance Paid time off Vision insurance Life insurance Qualifications Research project coordination Data entry Productivity software Full Job Description We are seeking an experienced and motivated Clinical Research Coordinator to help launch and grow an innovative clinical research site focused on improving patient care through cutting-edge clinical trials. This is an exciting opportunity to work alongside experienced physicians and healthcare professionals while helping bring new therapies and treatments to market. The ideal candidate is organized, compassionate, detail-oriented, and passionate about delivering exceptional patient care while ensuring regulatory compliance. Responsibilities Clinical Trial Coordination Coordinate all day-to-day activities for assigned clinical research studies. Schedule and conduct participant visits according to study protocols. Maintain study calendars and ensure all required procedures are completed on time. Assist investigators during participant visits and clinical assessments. Patient Recruitment and Retention Recruit and screen potential study participants. Coordinate informed consent with the Principal Investigator. Maintain excellent communication with participants throughout each study. Develop relationships with referral sources and physician offices to support enrollment. Regulatory Compliance Maintain Investigator Site Files and regulatory documentation. Ensure compliance with FDA regulations, ICH Good Clinical Practice (GCP), HIPAA, and Institutional Review Board (IRB) requirements. Prepare for sponsor monitoring visits and regulatory audits. Submit protocol amendments, continuing reviews, and required regulatory documentation. Data Management Complete accurate source documentation. Enter study data into electronic data capture (EDC) systems. Resolve sponsor queries promptly. Maintain complete and audit-ready participant records. Sponsor Relations Coordinate sponsor and CRO monitoring visits. Communicate regularly with sponsors regarding study progress. Assist with study start-up, enrollment, and closeout activities. Clinical Responsibilities Obtain vital signs. Collect laboratory specimens and process samples. Perform ECGs and other protocol-required procedures when appropriately trained. Monitor participants for adverse events and report concerns promptly. Administrative Duties Track enrollment goals and study milestones. Maintain study supplies and inventory. Participate in staff meetings and continuing education. Assist with study budgets and administrative tasks as needed. Qualifications Required Bachelor's degree in Nursing, Life Sciences, Healthcare Administration, or a related healthcare field, or equivalent clinical research experience. Minimum of 5 years of clinical research experience preferred. Strong organizational and communication skills. Ability to manage multiple clinical trials simultaneously. Proficiency with Microsoft Office. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP). Current Good Clinical Practice (GCP) certification. Experience with Electronic Data Capture (EDC) systems. Phlebotomy or clinical skills experience.

Pay:

$75,000.00 - $85,000.00 per year

Benefits:

Dental insurance Health insurance Life insurance Paid time off Vision insurance

Work Location:

In person