Daytona Clinic Positions (Future Openings • Connect Early)

This is an evergreen requisition. We don’t have an immediate opening, but we’re actively seeking talented professionals for upcoming opportunities. By applying, your information will be reviewed and considered for future roles as they become available.

About the role

K2 Medical Research is transforming healthcare by delivering tomorrow’s treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we lead multiphasic trials in therapeutic areas ranging from neurodegenerative to cardiometabolic medicine. Our culture is grounded in clinical excellence and a patient-first mission. We are seeking mission-driven individuals ready to play a meaningful role in bringing life-changing treatments to the patients who need them most.

These positions will support clinical trial performance at our Daytona Beach, FL clinic and ensure conduct is congruent with the philosophy and mission of K2 Medical Research. You will promote good clinical practices by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation.

Clinical Research Coordinator / Project Manager

Responsibilities

• Lead end-to-end execution of clinical trials, ensuring strict adherence to study protocols, GCP, and FDA guidelines
• Comprehensive management of assigned studies—from attending investigator meetings and coordinating with the Principal Investigator to managing complex communications with CROs, Sponsors, and monitors
• Perform clinical tasks such as phlebotomy and ECGs
• Administer psychiatric rating scales and maintain interrater reliability
• Manage study medication and source documentation
• Mentor staff and drive organizational momentum

Qualifications

• Bachelor’s degree required; Master’s degree highly preferred
• Strong medical or research experience
• Leadership skills
• Bilingual proficiency in Spanish and English is highly desired

Clinical Research Assistant

Responsibilities

• Provide vital operational support to the clinical team, assisting the Site Director and Project Managers in the daily execution of study protocols
• Maintain seamless communication between patients, study staff, and referral sources
• Ensure all documentation and sponsor queries are completed with high accuracy and timeliness
• Collect initial patient medical history
• Perform essential clinical tasks like vital signs and specimen packaging
• Educate patients and their families on the clinical trial process

Qualifications

• High school diploma required; Bachelor’s degree preferred
• Clinical background
• Prior research experience is ideal, but we value a combination of related education and a genuine passion for advancing medical research

Benefits

• Medical, dental, and vision options
• Supplemental insurance plans
• 401(k) with immediate employer match
• Generous paid time off and paid holidays

Schedule

Four-day work week consisting of 10-hour shifts from Monday through Thursday. Fridays are reserved only for critical business needs or administrative tasks; otherwise, they are your personal time.