Senior Clinical Research Monitor - Remote

Overview

As a Senior Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence.

In Short

• Field monitoring of studies and data collection for clinical trials.
• Assure compliance with protocols, GCP, and regulatory requirements.
• Develop and deliver technical training on GCPs and protocols.
• Act as a mentor to new or junior level employees.
• Provide oversight of trial activities and insights to principal investigators.
• Contribute to the development of clinical protocols and informed consent forms.
• Validate investigational device accountability.
• Verify trial/study data and maintain regulatory documents.
• Edit/amend informed consent documents.
• Travel up to 75% for clinical site visits.

Requirements

• Bachelor's Degree in related field or equivalent 5 years of clinical research monitoring experience.
• Experience in a regulated industry.
• Experience with electronic data capture.
• Covid Vaccination required.
• Knowledge of cardiovascular physiology preferred.
• Clinical research certification (ACRP or SOCRA) preferred.
• Excellent communication and analytical skills.
• Proven expertise in MS Office Suite.
• Technical writing skills are a plus.
• Ability to relate well with key opinion leaders.

Benefits

• Competitive salaries and performance-based incentives.
• Wide variety of benefits programs.
• Commitment to employee health and safety.
• Support for professional development.
• Equal Opportunity/Affirmative Action employer.