Remote Clinical Research Associate: Site Monitoring Expert

Merck & Co.; Rahway (NJ); Remote; USD 96,000 - 151,000; Full time

Job summary

Merck & Co. in Rahway, NJ seeks an experienced Clinical Research Associate to oversee monitoring across sites, ensure GCP compliance, and manage regulatory documentation. The role involves heavy travel and collaboration with SR teams to drive site readiness and data integrity.

Expect strong site management skills, familiarity with CTMS/eTMF, and the ability to handle complex regulatory requirements in a fast-paced environment.

Qualifications

• Associate's or higher in healthcare/science with relevant experience.
• At least 2 years direct site management/monitoring in pharma/CRO.
• Experience with ICH-GCP and regulatory documentation preferred.
• Immunology experience is a plus.

Responsibilities

• Ensure protocol conduct compliance and site oversight across studies.
• Manage sites, develop relationships and drive site readiness.
• Coordinate activities with sponsor, CRO, and site staff.
• Perform remote and on-site monitoring, ensure data integrity and patient safety.
• Collect regulatory docs, communicate issues, and support audits.

Skills

Site management

Monitoring

ICH-GCP

Regulatory knowledge

Education

Associate's degree in scientific/healthcare

Bachelor's degree or above

Tools

CTMS

eTMF

Regulatory docs

Job description

Merck & Co. in Rahway, NJ seeks an experienced Clinical Research Associate to oversee monitoring across sites, ensure GCP compliance, and manage regulatory documentation. The role involves heavy travel and collaboration with SR teams to drive site readiness and data integrity.

Expect strong site management skills, familiarity with CTMS/eTMF, and the ability to handle complex regulatory requirements in a fast-paced environment.