What are the responsibilities and job description for the Clinical Research Associate position at Warman O'Brien?
Clinical Research Associate II (CRA II) | North Carolina | Permanent | Hybrid
I'm currently supporting a leading global biopharmaceutical organisation in the search for a Clinical Research Associate II to join their expanding Clinical Operations team.
This is a fantastic opportunity for an experienced CRA looking to take the next step in their career with a company that is committed to advancing innovative therapies and improving patient outcomes worldwide.
You'll be responsible for managing site monitoring activities across the full clinical trial lifecycle, working closely with investigators and study teams to ensure studies are delivered to the highest quality standards. The role offers excellent exposure, autonomy, and the chance to work within a highly collaborative and supportive environment.
🔹 Independent site monitoring experience required
🔹 Strong understanding of ICH-GCP and clinical trial regulations
🔹 Opportunity to work on innovative clinical development programmes
🔹 Excellent career progression and long-term development opportunities
🔹 Competitive compensation, benefits, and supportive team culture
If you're a CRA who enjoys site relationships, values quality, and wants to work within a supportive, collaborative environment where your contribution is recognised, this could be the move you've been waiting for.
If you'd like to learn more, please send me a copy of your CV and I'll be in touch to arrange a confidential discussion.