What are the responsibilities and job description for the Clinical Research Coordinator position at SQRL?
HIGHLIGHTS
- Onsite Clinical Research Coordinator opportunity with our client in the greater Fleming Island area
- Monday through Friday schedule, 7:00 AM to 4:00 PM
- Competitive hourly pay based on experience plus strong benefits
- Work across Phase I-IV clinical trials with meaningful patient-facing responsibilities
- Strong career growth potential within a fast-growing research organization connected to 30 sites across 10 states
- Great fit for someone who enjoys patient care, organization, and a hands-on clinical research environment
COMPANY
Our client is a growing clinical research organization focused on helping bring new treatments and therapies to patients through high-quality clinical trials. They offer a supportive, team-oriented environment where employees can build their skills, take on more responsibility, and grow over time. As part of a larger and rapidly expanding network with more than 30 sites across 10 states, this role offers the chance to join an entrepreneurial organization with real long-term career development potential as growth continues in 2025 and beyond.
POSITION
The Clinical Research Coordinator will support the day-to-day execution of clinical trials while helping ensure a strong experience for study participants. This person will work closely with investigators, patients, sponsors, and internal staff to keep studies organized, compliant, and moving forward. The role is ideal for someone who is detail-oriented, comfortable in a clinical setting, and able to balance patient interaction with documentation and protocol responsibilities.
RESPONSIBILITIES
- Obtain informed consent and support study participants throughout the trial process
- Carry out protocol-related procedures carefully and according to study guidelines
- Perform clinical tasks such as vital signs, specimen collection and processing, and study-related lab shipment preparation
- Complete source documentation, adverse event reporting, and data entry in electronic systems
- Maintain study files, supplies, and overall organization for assigned trials
- Communicate with sponsors and CROs and assist with monitoring, initiation, and other site visits
QUALIFICATIONS
- Bachelor’s degree preferred, but not required
- Prior Clinical Research Coordinator experience preferred, ideally 2 years
- Hands-on clinical skills are strongly preferred, including phlebotomy, ECG/EKG, injections, and vital signs
- Working knowledge of GCP, FDA, ICH, and general clinical research standards
- Comfortable using electronic documentation platforms and Microsoft Office
- Strong communication, organization, critical thinking, and attention to det