The Quality Manager monitors data and clinical operations consistency across network sites to ensure adherence to ICH-GCP and regulatory standards. They are responsible for creating SOPs, conducting internal study reviews, and managing corrective and preventive action plans.
The Participant Marketing Coordinator manages the operational aspects of participant recruitment for clinical trials, including study start-up, budget oversight, and vendor coordination. They ensure marketing campaigns are launched on time, remain within budget, and comply with all regulatory requirements.
The specialist will manage accounts receivable, oversee study budgets, and ensure accurate revenue recognition. They will act as a liaison between clinical teams and sponsors to verify contractual performance and handle invoicing.
Responsible for identifying and screening potential clinical trial participants via outbound and inbound calls. Tasks include assessing eligibility based on protocol criteria and scheduling qualified candidates for on-site visits.
This strategic leadership role involves identifying, developing, and managing high-impact collaborations between the research network and biotechnology/pharmaceutical companies to drive revenue growth. The Director will act as the primary bridge between external innovators and clinical operations, ensuring sites remain partners of choice for cutting-edge trials.
