Senior Clinical Research Coordinator - Remote

Overview

The Senior Clinical Research Coordinator is responsible for planning, coordinating, and managing activities related to clinical trials while ensuring compliance with regulatory bodies and maintaining patient safety.

In Short

• Plans and coordinates clinical trial activities.
• Interfaces with clinical staff and external entities.
• Identifies eligible patients for trials.
• Provides education to hospital personnel and patients.
• Ensures compliance with protocols and regulatory agencies.
• Monitors patient participation and safety.
• Completes protocol budgeting and feasibility.
• Maintains communication with research administration.
• Performs other related duties as assigned.
• Adheres to ethical and legal standards.

Requirements

• Minimum Associate's degree or equivalent research experience.
• 3-5 years of related experience.
• Preferred Bachelor's Degree.
• Current research-related certification (e.g., CCRC, ACRP-CP).
• Driver's license may be required.
• Compliance with HIPAA and data security guidelines.

Benefits

• Opportunity to work with a leading health organization.
• Engagement in innovative health solutions.
• Comprehensive training and development opportunities.
• Supportive work environment focused on ethical practices.
• Access to a wide range of health-related services.