Serves as a scientific expert for clinical trials, liaises with key opinion leaders, and provides medical information.

Analyzes clinical trial data, prepares statistical reports, and collaborates with biostatisticians.

Manages clinical trials, coordinates with clinical sites, monitors trial progress, and ensures compliance with protocols.

Ensures quality standards in clinical trials, conducts audits, and manages quality control processes.

Monitors drug safety, processes adverse event reports, and ensures compliance with pharmacovigilance regulations.

Manages clinical trial data, designs databases, performs data validation, and ensures data integrity and accuracy.

Oversees regulatory submissions, ensures compliance with regulatory requirements, and communicates with regulatory agencies.

Prepares clinical documents, including study protocols, clinical study reports, and regulatory submission documents.

Manages clinical trial projects, coordinates with different teams, tracks project progress, and ensures timely completion.

Provides statistical support for clinical trials, including data analysis, designing studies, and preparing reports.