Senior Clinical Research Associate I

Role: Senior Clinical Research Associate I responsible for site management, monitoring, and trial close-out to ensure patient safety and quality in Pfizer-led clinical trials. Objectives include maintaining investigator site relationships, safeguarding trial integrity, and ensuring compliance with GCP, laws, and Pfizer standards. Responsibilities encompass overseeing site activities from initiation to database lock, serving as the primary site contact, providing protocol training, supporting recruitment, conducting onsite and remote monitoring, managing adverse event reporting, resolving site issues, and ensuring investigational product oversight. Qualifications: Bachelor's in life sciences, nursing, pharmacy or related field; minimum 3 years clinical research site monitoring experience, preferably in Oncology; strong knowledge of GCP, FDA, and local regulations; fluent in English and local language(s). Preferred: experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases; global trial experience; demonstrated ability to support regulatory interactions and manage complex issues. High-Value: Oncology/ infectious disease focus, clinical trial monitoring, site development, and compliance; extensive travel (60-80%), with some international travel. Work setup involves significant travel within the area, with a need for valid driver's license and passport.