Supports quality control activities, including testing products, conducting inspections, and ensuring compliance with quality standards. Requires background in quality control and strong attention to detail.

Supports the development of scientific communications, including preparing presentations, drafting reports, and liaising with stakeholders. Requires strong communication skills and a background in scientific writing.

Manages clinical operations, including trial design, execution, and monitoring. Ensures trials are conducted in compliance with protocols and regulatory requirements. Requires experience in clinical operations, project management skills, and the ability to oversee multiple trials simultaneously.

Monitors and manages drug safety data, including adverse event reporting and risk assessment. Ensures compliance with safety regulations and maintains up-to-date knowledge of safety standards. Requires experience in pharmacovigilance and a strong understanding of safety protocols.

Oversees the planning, execution, and monitoring of clinical trials. Manages trial budgets, timelines, and ensures adherence to protocol. Requires experience in clinical trial management, strong leadership, and project management skills.