Teams at K2 Medical Research

Administer, score, and interpret cognitive, diagnostic, clinical, and psychometric assessments for pharmaceutical clinical trials involving neurological and mental health conditions. Conduct caregiver interviews, telephone screens, and eligibility evaluations while following study protocols, FDA requirements, Good Clinical Practice, and company SOPs. Maintain accurate documentation, address queries, communicate rating issues, support participant safety, and supervise study lead and coordinator scheduling duties.

Provides medical oversight for clinical research patients and study teams. Reviews trial eligibility, conducts patient assessments and physical examinations, interprets laboratory results, EKGs, and safety data, monitors adverse events, ensures accurate documentation and protocol compliance, and collaborates with physicians, nurses, and research personnel. The role is onsite and full-time, with training provided and occasional travel for study-related meetings.

Performs quality control reviews of clinical research source documents, investigator site files, eligibility records, training documentation, and regulatory compliance. Coordinates with Quality Management and clinical sites to resolve issues, create queries, track compliance trends, report quality concerns, and provide staff training. The role requires hybrid clinic support in Florida, independent work, strong organizational and communication skills, and knowledge of clinical research regulations and SOPs.