Tampa Clinic Positions (Future Openings • Connect Early)

Overview

K2 Medical Research is actively seeking talented professionals for upcoming opportunities in clinical research. By applying now, your information will be reviewed and considered for future roles as they become available.

Responsibilities

• 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).
• Collect, record, and maintain source and sponsor documentation.
• Administer and interpret 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.
• Ensure data collection is in congruence with company philosophy and specific scale administration guidelines.
• Conduct diagnostic assessments and caregiver interviews, prevent rater drift, and supervise study lead duties for at least four studies.
• Takes a lead role in the end-to-end execution of clinical trials, ensuring strict adherence to study protocols, GCP, and FDA guidelines.
• Perform clinical tasks such as phlebotomy and ECGs, administer psychiatric rating scales, maintain interrater reliability, and manage study medication and source documentation.
• Maintain 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.
• Provide vital operational support to the clinical team, assisting the Site Director and Project Managers in the daily execution of study protocols.
• Serve as the initial bridge between potential participants and groundbreaking medical research at our clinic in The Villages, FL.
• Meticulously triage patients through medical and psychiatric interviews, record collection, and preliminary clinical assessments such as memory testing and vital signs.
• Act as a vital educator, guiding patients and their families through the complexities and requirements of the clinical trial process.

Qualifications

• Psychometric Rater: Minimum of a BS/BA in Psychology is required (Master’s preferred), along with at least 2 years of psychometric or clinical research experience. Certified Psychometrist and bilingual (English/Spanish) is strongly preferred.
• Clinical Research Coordinator/Project Manager: Bachelor’s degree, strong medical or neurodegenerative research experience (particularly in Parkinson’s), and leadership skills necessary to mentor staff and drive organizational momentum. Bilingual proficiency in Spanish and English is highly desired.
• Clinical Research Assistant: High school diploma (Bachelor’s preferred) and a clinical background; while prior research experience is ideal, we value a combination of related education and a genuine passion for advancing medical research.
• Prescreen Coordinator: Minimum of one year of clerical experience—ideally in a healthcare setting—who thrives in a fast-paced environment and is eager to ensure every data point is captured with precision to support the advancement of patient care.

Benefits

• Comprehensive benefits package including medical, dental, and vision options, supplemental insurance plans, 401(k) with immediate employer match, generous paid time off, and paid holidays.
• A four-day work week consisting of 10-hour shifts from Monday through Thursday, with Fridays reserved only for critical business needs or administrative tasks.