Teams at CenExel

Coordinates clinical trials from initiation through completion while maintaining ICH, GCP, protocol, and regulatory compliance. Responsibilities include scheduling data collection, organizing study information, documenting adverse events and protocol deviations, reporting research data, supporting regulatory activities, educating participants, and performing safety and efficacy assessments such as vital signs, EKGs, and blood draws.

Administers clinical, neurocognitive, behavioral, and functional assessments for clinical trial participants. Conducts interviews, scores rating scales, supports diagnosis and psychopathology evaluations, maintains data integrity, participates in consensus rounds, and follows study protocols, FDA regulations, ICH, GCP, and company procedures. The role also supports participant screening, study-specific training, documentation, and continuity of clinical ratings across neuroscience studies.

Coordinates clinical trial activities from initiation through completion, including patient scheduling, data collection, safety and efficacy assessments, regulatory documentation, adverse-event reporting, protocol compliance, and sponsor communication. Educates participants, organizes study information, maintains research quality, and supports clinical trial operations in accordance with ICH, GCP, federal regulations, and company policies.