Senior Clinical Research Associate

ICON seeks a Senior Clinical Research Associate to monitor a cardiovascular medical device study focused on atrial fibrillation. The role involves sponsor-dedicated support across multiple western U.S. regions, requiring extensive monitoring experience and expertise in FDA regulations and clinical trial management.

Responsibilities

• Monitor cardiovascular/electrophysiology medical device study sites for protocol compliance and data integrity
• Identify and mitigate risks at sites; implement effective solutions promptly
• Communicate complex trial information clearly to diverse stakeholder groups
• Establish and maintain effective working relationships with site staff, investigators, and internal teams
• Manage multiple priorities independently in a dynamic clinical research environment

Requirements

• 3+ years of clinical monitoring experience in cardiovascular medical devices or related pharma/electrophysiology
• Bachelor's degree in Life Science, Physical Science, Nursing, or Biological Science
• In-depth knowledge of FDA regulations and ICH/GCP guidelines
• Strong problem-solving and interpersonal skills with site personnel and investigators
• Exceptional verbal and written communication abilities
• Located in western U.S. near major airport; able to travel up to 65% regionally
• Clinical trial management expertise with rigorous attention to detail

Compensation: $110,520–$138,150 base