You will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability
Job Summary
You will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability.
You will serve as a Subject Matter Expert (SME), contribute to regional process improvements, and partner directly with Site Care Partners on early-phase activation activities.
Your deep therapeutic insight and leadership will directly safeguard trial integrity, strengthen crucial investigator relationships, and enhance Pfizer's scientific credibility.
Matching Summary
You will oversee site management, monitoring, and close-out operations for assigned clinical trials with a higher level of accountability.
Skills & Requirements
Must-have
Site management
Monitoring operations
Compliance with GCP
Mentorship responsibilities
Global clinical trial experience
Fluency in English
Advanced analytical capacity
Nice-to-have
Oncology experience
Vaccines expertise
Internal medicine knowledge
Infectious diseases background
Key Requirements
Bachelor’s degree in Life Sciences or equivalent
Minimum of 3 years of relevant experience in clinical research site monitoring
Prior global clinical trial experience required
Fluency in English and native language(s) of the country