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Clinical Research Associate
New York, United States · À temps plein
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- Expérience
- 5+ yrs
- Salaire
- —
- Ouvertures
- 1
- Publié
- il y a 1 heure
- Work mode
- Au bureau
- Resume
- Required to apply
Where you'll work
Description de l'emploi
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.