Tampa Clinical Positions

K2 Staffing LLC•Tampa, FL

3d•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, Prescreen Coordinators, & Psychometric Raters to potentially support our clinic out of Tampa, 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

Minimum of a BS/BA in Psychology (Master’s preferred) for Psychometric Rater.
At least 2 years of psychometric or clinical research experience for Psychometric Rater.
Bachelor’s degree for Clinical Research Coordinator/Project Manager.
Strong medical or neurodegenerative research experience (particularly in Parkinson’s) for Clinical Research Coordinator/Project Manager.
Leadership skills necessary to mentor staff and drive organizational momentum for Clinical Research Coordinator/Project Manager.
High school diploma (Bachelor’s preferred) for Clinical Research Assistant.
Clinical background for Clinical Research Assistant.
Minimum of one year of clerical experience—ideally in a healthcare setting—for Prescreen Coordinator.
Dependable, customer-service-oriented professional for Prescreen Coordinator.
Ability to thrive in a fast-paced environment for Prescreen Coordinator.
Eagerness to ensure every data point is captured with precision to support the advancement of patient care for Prescreen Coordinator.

Nice To Haves

Certified Psychometrist for Psychometric Rater.
Bilingual (English/Spanish) for Psychometric Rater.
Bilingual proficiency in Spanish and English for Clinical Research Coordinator/Project Manager.
Prior research experience is ideal for Clinical Research Assistant, but a combination of related education and a genuine passion for advancing medical research is valued.

Responsibilities

Administering and interpreting quantitative and qualitative tests as part of a clinical team investigating treatments for disease states including Alzheimer’s, Mild Cognitive Impairment, Depression, and Parkinson’s.
Ensuring data collection is in congruence with company philosophy and specific scale administration guidelines.
Conducting diagnostic assessments and caregiver interviews.
Preventing rater drift.
Supervising study lead duties for at least four studies.
Taking a lead role in the end-to-end execution of clinical trials, ensuring strict adherence to study protocols, GCP, and FDA guidelines.
Performing 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.
Managing study medication and source documentation.
Providing 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.
Serving as the initial bridge between potential participants and groundbreaking medical research.
Meticulously triaging patients through medical and psychiatric interviews, record collection, and preliminary clinical assessments such as memory testing and vital signs.
Data entry and schedule management.
Educating patients and their families through the complexities and requirements of the clinical trial process.