Senior Clinical Research Associate

IRE • Los Angeles, CA

10d • Remote

About The Position

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib. The ideal candidate will have cardiovascular medical device monitoring experience- however, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience will be considered.

Requirements

• 3 years of monitoring experience required.
• Bachelor’s degree required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
• In-depth knowledge of FDA regulations and ICH/GCP guidelines.
• Strong problem-solving skills.
• Strong interpersonal skills.
• Exceptional verbal and written communication skills.
• Ability to tailor communication style to the needs and preferences of different stakeholders.
• Ability to work independently.
• Must have the legal right to work in the country where the role is based.

Nice To Haves

• Cardiovascular medical device monitoring experience.
• Complex experience in cardiovascular/electrophysiology pharma monitoring.
• Coordinator/Nursing experience.

Responsibilities

• Monitor clinical trials in the cardiovascular/electrophysiology medical device space, with a focus on A-fib indication.
• Mitigate risks and identify issues at sites, implementing effective solutions promptly.
• Establish and maintain effective working relationships with site personnel, investigators, and internal teams.
• Communicate complex information clearly and concisely to various stakeholders.
• Manage multiple priorities in a dynamic environment.
• Execute a well-defined plan for communication with study teams and sites.
• Manage clinical trials effectively.
• Prepare rigorous, detailed, and precise reports.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Senior