Clinical Research Associate

Role: Clinical Research Associate responsible for site management and monitoring of clinical trials to ensure patient safety, data quality, and compliance with GCP, regulations, and Pfizer standards. Responsibilities include site initiation, routine and remote monitoring, addressing protocol issues, managing investigator relationships, supporting patient recruitment, conducting site close-outs, and ensuring investigational product oversight. The role involves troubleshooting site issues, training, and maintaining study documentation, with a focus on recruiting in oncology, vaccines, or infectious diseases. Qualifications: Bachelor's degree in life sciences or related fields, at least 1 year of clinical research monitoring experience, knowledge of ICH/GCP, FDA, and local regulations, and fluency in English and local languages. Preferred experience in global trials within oncology, vaccines, or infectious diseases. The position requires significant travel (60-80%) and a valid driver’s license and passport. The role demands strong communication, analytical skills, and ability to work in a matrix team environment. It is based in the U.S., with competitive salary and benefits, and no current visa sponsorship available.