Nashville Clinic Positions (Pooling)

K2 Staffing LLC•Berry Hill, TN

8h•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 Psychometric Raters and Clinical Research Coordinator/Project Managers, to potentially support our clinic out of Nashville, TN. 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).
At least 2 years of psychometric or clinical research experience.
Bachelor’s degree.
Strong medical or research experience.
Leadership skills necessary to mentor staff and drive organizational momentum.

Nice To Haves

Certified Psychometrist
Bilingual (English/Spanish)
Bilingual proficiency in Spanish and English
Master's level degree highly preferred.

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.
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.