Senior Clinical Research Associate

About the role

The Senior Clinical Research Associate will manage site monitoring, activation, and close‑out for assigned investigator sites, ensuring patient safety and high‑quality study execution in line with GCP, regulatory requirements and Pfizer standards.

Key responsibilities

• Manage and monitor assigned investigator sites throughout the clinical trial lifecycle, including on‑site, remote and electronic visits.
• Support site activation, patient recruitment, enrollment, and study progress, and maintain all study documentation and Trial Master File records.
• Review adverse events, resolve data queries, oversee investigational product management and support database release activities.
• Identify site‑level issues, implement corrective actions, and contribute to audit readiness and quality remediation.

Required profile

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Medicine or related field.
• Minimum 3 years of clinical research site monitoring experience, preferably in Oncology, Vaccines, Internal Medicine or Infectious Diseases.
• Global clinical trial experience with fluency in English and the local language of the employment country.
• Willingness to travel extensively, including occasional international and weekend travel, with a valid driver’s license and passport.

Required skills

• Strong knowledge of clinical trial methodologies, ICH/GCP and FDA regulations.
• Ability to evaluate, interpret and communicate complex clinical and operational issues.
• Effective stakeholder management and communication in a matrix environment.