Clinical Research Coordinator 2 - Remote

Overview

The Clinical Research Coordinator 2 position involves managing and coordinating clinical research projects, ensuring compliance with regulatory standards, and supporting the recruitment and monitoring of study subjects.

In Short

• Conduct site qualifications and study initiation.
• Maintain regulatory documents and coordinate study conduct.
• Recruit eligible study subjects and manage informed consent.
• Abstract and document clinical research data.
• Monitor adverse events and ensure protocol adherence.
• Facilitate quality assurance reviews.
• Work independently and as part of a team.
• Communicate effectively with study teams and subjects.
• Handle sensitive matters with discretion.
• Perform various tasks in moderately complex clinical studies.

Requirements

• Bachelor's degree in a related field.
• 2-5 years of relevant work experience.
• Clinical research experience preferred.
• Ability to manage multiple studies simultaneously.
• Strong communication and interpersonal skills.
• Detail-oriented and able to prioritize tasks.
• Ability to work independently with minimal supervision.
• Knowledge of regulatory compliance and safety protocols.
• Ability to handle stressful situations effectively.
• Commitment to confidentiality and discretion.

Benefits

• Comprehensive health benefits.
• Retirement plans.
• Paid time off.
• Professional development opportunities.
• Diverse and inclusive work environment.
• Access to university resources and programs.
• Support for work-life balance.
• Opportunities for academic engagement.
• Employee assistance programs.
• Competitive salary range.