This is a fully remote position, open to applicants in South Korea.

📋 Description

• Ensure the appropriate execution of clinical trials in compliance with relevant laws, Good Clinical Practices, and Pfizer standards.

• Act as the main point of contact for designated investigator sites.

• Perform onsite and remote/electronic monitoring as required for study site activities.

• Oversee site-level adverse events (AEs) and serious adverse events (SAEs) while collaborating with the Drug Safety Unit.

• Submit all necessary reports, documentation, and updates within stipulated timeframes.

• Identify and address issues at investigator sites within required timeframes.

• Ensure the quality of site delivery.

⛳️ Requirements

• Bachelor's degree in life sciences or a related professional degree.

• Comprehensive understanding of clinical trial methodologies, ICH/GCP, FDA, and local country regulations.

• At least 3 years of relevant experience in clinical research site monitoring, preferably with 2 years in Oncology.

• Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.

• Must be proficient in English and the native language(s) of the country in which they will operate.

🏝️ Benefits

• Remote work options.