Senior Clinical Research Coordinator - Remote

Overview

The Senior Clinical Research Coordinator (Sr CRC) is a specialized research professional working under the direction of the clinical Principal Investigator (PI), overseeing and coordinating the daily activities of complex clinical trials to ensure compliance with regulations.

In Short

• Lead within the department to improve clinical research practices.
• Maintain knowledge of current protocols and internal SOPs.
• Accountable for high standards in clinical research practice.
• Develop and implement procedures for data collection and quality assurance.
• Assist with regulatory documentation and audits.
• Provide guidance to investigators regarding protocol requirements.
• Facilitate daily activities of complex clinical studies.
• Use knowledge of clinical studies to coordinate data collection.
• Train junior CRCs and handle competing demands effectively.
• Participate in continuing education relevant to the role.

Requirements

• College or university degree in a related field.
• 5-7 years of work experience in a related job discipline.
• Preferred: Bachelor's degree and research certification.
• Familiarity with medical terminology and clinical trial protocols.
• Working knowledge of Good Clinical Practices (GCP).
• Extensive knowledge of Microsoft Word, Excel, and Adobe Acrobat.
• Excellent interpersonal and data management skills.
• Ability to prioritize work assignments and manage time effectively.
• Experience coordinating multiple studies, including investigator-initiated trials.

Benefits

• Comprehensive health, retirement, and paid time off benefits.
• Opportunities for professional development and training.
• Supportive work environment promoting collaboration.
• Participation in a leading research institution.
• Flexibility with hybrid work arrangements.