Clinical Research Coordinator

About Sarasota Arthritis Center

Established in 1977, Sarasota Arthritis Center is a privately owned, physician-led rheumatology practice serving Southwest Florida, with locations in Sarasota, Venice, and Bradenton. We provide comprehensive rheumatology care, including on-site infusion therapy and clinical research. Built on a longstanding foundation of compassion, integrity, and excellence in patient care, we foster a supportive, team-oriented environment where employees are valued, collaboration is encouraged, and patients remain at the center of everything we do.

Overview

The Clinical Research Coordinator (CRC) is responsible for coordinating and conducting clinical research trials within Sarasota Arthritis Center in accordance with study protocols, regulatory requirements, ICH/GCP guidelines, and site standard operating procedures (SOPs).

This is a hands-on clinical research role requiring prior Clinical Research Coordinator experience. The CRC works closely with Principal Investigators, study participants, sponsors, Contract Research Organizations (CROs), and the clinical research team to ensure studies are conducted safely, efficiently, accurately, and in compliance with all applicable requirements.

Why Join Sarasota Arthritis Center?

Sarasota Arthritis Center offers a comprehensive benefits package and a work environment designed to support both professional success and work/life balance, including:

• 100% employer-paid medical insurance for employee-only coverage
• 401(k) with company match and employer-funded profit sharing
• Four-day workweek (Monday–Thursday) supporting a healthy work/life balance
• Paid holidays and Paid Time Off (PTO)
• Collaborative, team-oriented culture with strong support and a shared commitment to exceptional patient care

Key Responsibilities

Clinical Trial Coordination & Study Management

• Coordinate assigned clinical research studies from site initiation through study close-out.
• Review and interpret study protocols and ensure study activities are conducted in accordance with protocol requirements, IRB requirements, FDA regulations, ICH/GCP guidelines, and site SOPs.
• Coordinate and conduct participant study visits according to protocol.
• Perform clinical research procedures within the scope of RN licensure and study requirements, including vital signs, blood draws, specimen collection and processing, EKGs, injections, IV placement, and other protocol-specific assessments.
• Administer and monitor IV infusions and investigational products as permitted by study protocol, site policy, and applicable regulations.
• Monitor participants during and following infusions and other study procedures and appropriately identify, document, and escalate adverse events or changes in clinical status.
• Ensure informed consent is appropriately obtained and documented prior to conducting study-related procedures.
• Maintain accurate, complete, and timely source documentation and study records.
• Enter study data into electronic data capture (EDC) systems and respond to data queries within required timelines.
• Coordinate participant scheduling, follow-up visits, laboratory testing, imaging, and other study-related activities.
• Monitor participant recruitment and retention and assist with strategies to achieve study enrollment goals.
• Ensure study-related equipment is properly maintained, calibrated, and documented as required.
• Ensure investigational products are received, stored, handled, administered, and documented in accordance with Good Clinical Practice, applicable regulations, and protocol requirements.

Regulatory Compliance & Quality

• Assist with the preparation, submission, and maintenance of regulatory documents, including IRB submissions, amendments, continuing reviews, and study close-out documentation.
• Maintain investigator site files, regulatory binders, delegation logs, training records, and study correspondence.
• Maintain required study-specific, GCP, and regulatory training.
• Assist with sponsor monitoring visits, audits, and regulatory inspections.
• Address monitoring findings and queries promptly and accurately.
• Ensure assigned studies remain in a state of inspection readiness.
• Report protocol deviations, adverse events, serious adverse events, and other reportable events according to protocol and regulatory requirements.

Collaboration & Communication

• Serve as a key point of contact for assigned studies with sponsors, CROs, monitors, vendors, and study participants.
• Work closely with Principal Investigators and other research team members to ensure appropriate study oversight and timely completion of study activities.
• Collaborate with physicians, advanced practice providers, nurses, medical assistants, and administrative staff to integrate research activities into clinical operations.
• Maintain clear, professional, and compassionate communication with study participants regarding appointments, study requirements, instructions, and follow-up.
• Communicate study concerns, participant safety issues, protocol deviations, and operational challenges promptly to the appropriate Principal Investigator and research leadership.

Research Operations

• Participate in feasibility assessments and site qualification activities for potential new clinical trials.
• Assist with study start-up activities, including site initiation visits, staff training, and preparation of study materials.
• Assist with maintaining and updating Research Department SOPs and processes.
• Support accurate tracking of study-related activities, billing, invoicing, and sponsor payments as assigned.
• Maintain confidentiality of participant information and comply with HIPAA and all applicable privacy requirements.
• Support departmental quality improvement initiatives and other research-related projects as needed.

Other duties as assigned. This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

Qualifications

• 3+ years of clinical research experience.
• Previous professional experience working as a Clinical Research Coordinator (CRC) in clinical trials
• Clinical experience with blood draws, specimen collection, injections, and other common clinical procedures.
• Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research requirements.
• Experience coordinating clinical trials and working with study protocols, informed consent, source documentation, and regulatory documentation.
• Strong organizational skills and exceptional attention to detail.
• Ability to manage multiple studies, priorities, deadlines, and participant schedules simultaneously.
• Strong clinical judgment and ability to recognize and appropriately escalate participant safety concerns.
• Excellent written and verbal communication skills.
• Ability to work collaboratively with physicians, research staff, sponsors, CROs, monitors, and study participants.
• Proficiency with electronic medical records, electronic data capture systems, and standard computer applications.
• Clinical research experience in rheumatology, autoimmune disease, infusion therapy, or specialty medicine preferred.
• Experience working on pharmaceutical or industry-sponsored clinical trials preferred.
• Clinical Research Coordinator certification through ACRP (CCRC) or SoCRA (CCRP) preferred.
• Current and unrestricted Registered Nurse (RN) / Licensed Practical Nurse (LPN) license in the State of Florida preferred.
• IV Certification preferred.
• Experience with investigational product accountability and administration preferred.
• Experience participating in sponsor monitoring visits, audits, and/or regulatory inspections preferred.

Equal Employment Opportunity

Sarasota Arthritis Centers provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.