Assists in the planning, implementation, and monitoring of clinical trials. Ensures adherence to study protocols, collects data, and maintains accurate records. Works with investigators to resolve issues and ensures compliance with regulatory requirements. Conducts site visits and audits, and prepares reports on study progress.

Supports research activities, including conducting experiments, analyzing data, and documenting results. Requires a background in pharmaceutical research and laboratory experience.

Helps monitor and manage drug safety data, including adverse event reporting and risk assessment. Requires knowledge of safety regulations and strong analytical skills.

Oversees regulatory submissions and ensures compliance with local and international regulations. Manages the preparation of regulatory documents and interacts with regulatory agencies. Requires extensive knowledge of regulatory requirements, strong communication skills, and experience in regulatory affairs.

Ensures that pharmaceutical products meet quality standards and regulatory requirements. Involves conducting inspections, audits, and quality control measures. Requires experience in quality assurance and knowledge of regulatory compliance.