Assists in evaluating drug safety data, including risk assessment and adverse event reporting. Requires background in drug safety and experience with safety evaluation processes.

Assists in ensuring that healthcare practices and processes comply with regulatory requirements and internal policies. Requires knowledge of compliance standards and strong attention to detail.

Oversees the collection, management, and analysis of clinical trial data. Ensures data accuracy, integrity, and compliance with study protocols. Requires experience in clinical data management, proficiency with data management systems, and strong organizational skills.

Studies the effects and mechanisms of drugs, including pharmacokinetics and pharmacodynamics. Conducts research on drug interactions, efficacy, and safety. Requires a Ph.D. in pharmacology or a related field, strong research skills, and experience in drug development.

Oversees regulatory submissions and ensures compliance with local and global regulations. Requires in-depth knowledge of regulatory guidelines, experience in dossier submission, and strong attention to detail. Must coordinate with regulatory bodies.