Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Senior Clinical Research Coordinator Amavita Research Services, LLC / Research Siter North Miami Beach, FL Job Details Full-time | Contract $60,000 - $80,000 a year 20 hours ago Benefits Health insurance 401(k) Career development plan Flexible schedule Qualifications BLS Certification HIPAA Project coordination ACLS Certification Research project coordination Health information regulatory compliance Bachelor's degree in nursing Clinical quality assurance standards FDA regulations
Full Job Description Senior Clinical Research Coordinator Job Category :
Healthcare Location :
North Miami Beach, FL Job Type:
Contract 1099,
Full-time Role Schedule :
Full-time | Monday-Friday, 8:00 a.m.-4:30 p.m.
Compensation :
$60,000 - $80,000 annually (commensurate with experience) + bonus eligibility About Us Amavita Research Services, LLC is a high-volume, Cardiovascular research center recognized for excellence in clinical trials with direct access to Advanced Cardiovascular of Miami — South Florida's only dedicated cardiovascular and interventional-radiology ambulatory surgery center. A next-generation cath lab built for advanced same-day procedures. We partner with leading sponsors and CROs to bring innovative therapies to patients while upholding the highest standards of regulatory compliance and patient safety. We are seeking a dedicated Senior Clinical Research Coordinator to join our team in a contractor role. The role of the Senior Clinical Research Coordinator is of great importance within our team and is an essential part of our organization. As a Senior Clinical Research Coordinator you should have with extensive clinical research experience. While cardiovascular expertise is preferred, it is not mandatory. The ideal candidate will independently manage the day-to-day trial conduct from activation through close-out, overseeing subject visits, data capture, compliance, and mentoring of junior staff.. If you thrive in a fast-paced environment and possess a strong desire to learn and grow continuously, our organization is the perfect place for you. Join our team and embrace the exciting journey of professional development!
Key Responsibilities :
Serve as the primary coordinator for multiple concurrent clinical trials (industry and investigator-initiated). Oversee subjects' screening, informed consent, study assessments, and AE/SAE reporting according to protocol requirements. Perform study procedures, such as ECGs and venipuncture/IV placement, laboratory samples processing, support with devices studies in cath lab and ensure proper accountability of investigational products or devices. Enter data into the Electronic Data Capture (EDC) system (e.g., Medidata Rave, Medrio, Oracle Cloud) and resolve queries in a timely manner. Coordinate sponsor/CRO monitoring visits and FDA audits, and assist in responding to findings and implementing CAPAs. Track study metrics—including enrollment, retention, and protocol deviations—and support accurate contract billing compliance. Train and mentor junior coordinators, and provide support to the Principal Investigator and sub-investigators. Required Qualifications. Degree in Nursing, Medicine, or a related medical field (a solid medical background is required) Extensive hands-on coordination of clinical trials with demonstrated mastery of Good Clinical Practice (GCP), HIPAA, and FDA regulations. Proficiency in electronic regulatory platforms and EDC systems. Current BLS certification; ACLS certification is a plus. Excellent communication skills and ability to interact effectively with sponsors, CROs, and regulatory authorities. Ability to work on-site in North Miami Beach, FL; occasional travel to investigator meetings as needed. Cardiovascular research experience is preferred but not required.
Compensation & Benefits :
This is a 1099 independent contractor position, offering competitive compensation between $60,000 and $80,000 annually, plus performance-based bonus opportunities. While traditional employee benefits (such as health insurance or 401(k)) are not provided, additional compensation or stipends may be negotiated based on project requirements. Flexible work arrangements with on-site responsibilities in North Miami Beach, FL, and potential for professional growth through additional assignments or contract extensions. How to
Apply :
Please submit your résumé/CV and a brief cover letter via Indeed or email to [• ]• with the subject line " Senior Clinical Research Coordinator Application." Applications will be considered based on relevant clinical research experience.
