| Location | NY |
| Salary | $100,000–$135,000 Per Year |
Responsibilities: of the Clinical Research Associate: Conduct site monitoring visits (on-site and remote) for cardiology or neurology clinical trials to ensure protocol adherence, GCP compliance, and data integrity. Review and verify clinical data, source documentation, and case report forms (CRFs/eCRFs). Ensure patient safety through adverse event reporting, serious adverse event follow-up, and safety documentation review. Collaborate with investigators, site staff, and cross-functional clinical teams to support study execution. Identify, document, and resolve site issues, protocol deviations, and data queries in a timely manner. Assist with site initiation, interim monitoring, and close-out visits. Maintain accurate trial master file (TMF) documentation and monitoring reports. Requirements of the Clinical Research Associate: Bachelor's degree in Life Sciences, Nursing, or a related field. 2+ years of Clinical Research Associate experience monitoring clinical trials. Hands-on experience with cardiology and/or neurology therapeutic areas. Strong knowledge of ICH-GCP guidelines and FDA regulations. Experience working with EDC systems, CTMS, and eTMF platforms. Ability to travel 8-10 days per month required by study needs. Excellent communication, organizational, and problem-solving skills. Compensation: for the Clinical Research Associate: $100,000 - $135,000 base salary Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.