Senior Clinical Research Associate I

Salary

Core Qualifications

Key Responsibilities

• •Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.
• •Ensure patient safety and compliance with informed consent and protocol requirements.
• •Review source documents and verify data integrity on Case Report Forms (CRFs).
• •Prepare accurate and timely monitoring reports and maintain study files.
• •Serve as lead monitor for assigned protocols and assist in developing monitoring plans.
• •Coordinate with vendors and internal teams to meet project timelines and objectives.
• •Support feasibility assessments, budget negotiations, and regulatory submissions.
• •Mentor and train junior team members through co-monitoring and guidance.
• •Travel extensively (60–80%) to support site activities and maintain audit readiness.