Perform site monitoring and site management tasks for a variety of protocols, sites, and therapeutic areas.
Conduct site monitoring visits (site selection, initiation, monitoring, and close-out visits) in accordance with the contractual scope of work and regulatory requirements.
Work with sites to tailor, implement, and monitor subject recruitment plans according to project needs to improve predictability.
Manage protocol
and study-related training for assigned sites and maintain regular communication with sites.
Assess the quality and integrity of study site practices.

Bachelor’s degree in a scientific discipline or healthcare preferred.
Minimum of 3 years of on-site monitoring experience required.
Thorough knowledge of and ability to apply applicable regulatory requirements for clinical research, e.g., Good Clinical Practice (GCP) and ICH guidelines.
Strong therapeutic and protocol knowledge as provided through company training.
Computer skills, including proficiency with Microsoft Word, Excel, and PowerPoint, and use of a laptop, iPhone, and iPad.
Written and verbal communication skills, including a good command of English.
Strong organizational and problem-solving skills.
Effective time management and financial resource management skills.
Ability to establish and maintain effective working relationships with colleagues, managers, and clients.

Senior Clinical Research Associate, Sponsor Dedicated

Key skills