Senior Clinical Research Associate II – Oncology

This is a fully remote position, open to applicants in New Jersey, +2 more states.

📋 Description

• Accountable for all facets of study site monitoring, including routine oversight and closure of clinical sites.

• Perform pre-study and initiation visits.

• Ensure that study personnel possess the necessary materials and instructions.

• Confirm adherence to informed consent procedures and study protocols.

• Monitor data for any missing or implausible entries.

⛳️ Requirements

• A university or college degree, or certification in a related allied health profession from a recognized institution (e.g., nursing licensure).

• Over 5 years of experience in Clinical Monitoring.

• Experience in oncology, particularly in early-phase studies, is preferred.

• Willingness to travel overnight 30-50% of the time.

🏝️ Benefits

• Health insurance coverage.

• 401(k) retirement plan.

• Paid time off.

• Options for remote work.

• Opportunities for professional development.