Clinical Research Associate

Role overview

A growing CRO is seeking an experienced Clinical Research Associate to help run a migraine-focused clinical study. This position is based in New York and is suited to someone who can oversee on-site study activities and support trial execution end to end.

Key responsibilities

• Carry out monitoring visits at study sites, including site initiation visits, interim monitoring visits, and close-out visits.
• Keep all study activities aligned with the protocol and ICH-GCP standards.
• Develop and maintain effective working relationships with investigators and site personnel.
• Examine study data and work through site-related queries to keep records accurate and complete.
• Assist with site performance management and efforts to improve patient recruitment.

Required profile

• Applicants should bring at least 5 years of experience working as a Clinical Research Associate.
• A solid grasp of ICH-GCP guidelines is essential.
• The role requires flexibility and willingness to travel whenever needed.

About the opportunity

This is a strong chance to join a growing organization and contribute to research aimed at improving outcomes for people living with migraine.