Daytona Clinic Positions (Pooling)

K2 Staffing LLC•Daytona Beach, FL

11d•Onsite

About The Position

This is an evergreen requisition, meaning 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. If you're interested in a future with K2 Medical Research, we encourage you to apply! At K2 Medical Research, we are 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. K2 is pooling for experienced Clinical Research Coordinator/Project Managers, & Clinical Research Assistants to potentially support our clinic out of Daytona Beach, FL. These positions will support clinical trial performance and ensure conduct is congruent to the philosophy and mission of K2 Medical Research. Promote good clinical practices in the conduct of clinical investigations 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.

Requirements

Bachelor’s degree
Strong medical or research experience
Leadership skills necessary to mentor staff and drive organizational momentum.
High school diploma (Bachelor’s preferred)
Clinical background
Combination of related education and a genuine passion for advancing medical research.

Nice To Haves

Bilingual proficiency in Spanish and English is highly desired.
Master's level degree highly preferred.
Prior research experience is ideal.

Responsibilities

Takes a lead role in the end-to-end execution of clinical trials, ensuring strict adherence to study protocols, GCP, and FDA guidelines.
Responsible for the comprehensive management of assigned studies—from attending investigator meetings and coordinating with the Principal Investigator to managing complex communications with CROs, Sponsors, and monitors.
Performing clinical tasks such as phlebotomy and ECGs, administering psychiatric rating scales, maintaining interrater reliability, and managing study medication and source documentation.
Provides vital operational support to the clinical team, assisting the Site Director and Project Managers in the daily execution of study protocols.
Maintaining a seamless flow of communication between patients, study staff, and referral sources while ensuring all documentation and sponsor queries are completed with high accuracy and timeliness.
Collecting initial patient medical history.
Performing essential clinical tasks like vital signs and specimen packaging.
Educating patients and their families on the clinical trial process.