The Clinical Trial Manager oversees clinical and operational activities for assigned studies, ensuring compliance with regulatory guidelines and internal SOPs. They manage study documentation, monitor site performance, mentor CRAs, and coordinate cross-functional teams to meet budget and timeline goals.
The Clinical Scientist/Rater Trainer develops and delivers rater training materials and provides protocol-specific training for clinical outcome assessments. They also evaluate rater performance, ensure scoring accuracy, and provide scientific expertise to study teams and investigators.
The QA Manager oversees clinical quality assurance activities, ensuring compliance with ICH GCP and internal QMS standards. They lead audits, manage CAPA processes, and drive continuous improvement initiatives across clinical programs.
Oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and sites to ensure data integrity and participant safety. Responsibilities include site initiation, monitoring, close-out, and mentoring junior staff.
The Director will plan and direct all accounting operations, including the month-end close, budgeting, and financial reporting. They are responsible for maintaining internal controls, ensuring regulatory compliance, and providing financial analysis to executive leadership.
Oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and sites to ensure data integrity and participant safety. Responsibilities include site initiation, monitoring, close-out, and mentoring junior staff.
The Director of Business Development is responsible for driving long-term growth by targeting the biopharmaceutical market in CNS and managing the full sales cycle from prospecting to closure. This includes developing strategic business plans, organizing sales campaigns with internal experts, and maintaining key client relationships.
