Clinical Research Associate (CRA) – Clinical Trials

About the role

As a Clinical Research Associate (CRA) at Pfizer, you will support the execution of clinical trials, ensuring data accuracy and regulatory compliance. Your work will directly contribute to the development of new medicines that improve patient outcomes.

Key responsibilities

• Coordinate and support day‑to‑day clinical trial activities, assisting managers with execution and milestone tracking.
• Maintain the Pfizer Trial Master File (PTMF) in line with ICH‑GCP and internal SOPs.
• Update trial and site information in the Corporate Clinical Trial Registry and assist with submissions to ethics committees and regulatory authorities.
• Provide administrative support for protocols and Informed Consent Documents, preparing materials for sites and ensuring timely delivery.
• Develop and maintain local tracking spreadsheets for study documents, data, and activities.
• Identify process improvements to enhance inspection readiness and PTMF compliance.

Required profile

• Bachelor’s degree (BA/BS) with any amount of relevant experience.
• Proven ability to introduce new ideas and follow Standard Operating Procedures.
• Strong organizational skills, attention to detail, and the capacity to prioritize multiple tasks.
• Excellent written and verbal communication skills.

Required skills

• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).
• Experience using Electronic Data Capture (EDC) systems and other clinical trial applications.