Assists in managing and analyzing research data related to pharmaceuticals, including data entry, validation, and reporting. Requires experience with data management systems and strong analytical skills.

Assists in medical affairs activities, including supporting medical information requests, preparing medical materials, and collaborating with healthcare professionals. Requires knowledge of medical affairs and strong communication skills.

Supports regulatory submission processes, helps prepare and review regulatory documents, and ensures compliance with guidelines. Requires knowledge of regulatory requirements and strong attention to detail.

Ensures that pharmaceutical products meet quality standards and regulatory requirements. Conducts inspections, quality control tests, and audits. Requires experience in quality assurance, knowledge of GMP (Good Manufacturing Practice), and strong attention to detail.

Analyzes statistical data from clinical trials and research studies, ensuring accurate interpretation and reporting. Requires expertise in statistical methods, data analysis, and proficiency with statistical software tools.