Parexel is seeking a Senior Clinical Research Associate to oversee the site management and monitoring throughout clinical trials. The role requires ensuring compliance with clinical practices and maintaining relationships with investigator sites for effective trial delivery. Candidates should possess extensive clinical trial knowledge, with at least 3 years of monitoring experience and a degree in life sciences.

The position involves travel of 60-80% and requires fluency in English. Parexel values diversity and is an equal opportunity employer.