Senior CRA role at ICON: Lead complex clinical trial sites, mentor teams, and ensure GCP compliance. 5+ yrs CRA exp & 60% travel required. Advance your career with a global leader.
Lead the Future of Clinical Research from the Field
At ICON, we are at the forefront of clinical development, transforming scientific discovery into life-saving therapies. Our success relies on the expertise of seasoned professionals who ensure integrity, quality, and excellence at every investigative site.
We are seeking a strategic and influential Senior Clinical Research Associate (SCRA) to elevate our clinical trial execution. In this pivotal field-based role, you will be entrusted with our most complex and high-priority sites. Beyond monitoring, you will act as a mentor, a strategic advisor, and a key driver of study success. If you are ready to leverage your deep expertise to lead sites, develop talent, and shape clinical operations, this is your opportunity to make a lasting impact.
Your Mission: Strategic Partner, Expert Mentor, Quality Champion
As a Senior CRA, you are the cornerstone of site excellence. You will manage critical site relationships, provide expert guidance, and ensure uncompromising compliance, all while mentoring the next generation of clinical research professionals.
Key Responsibilities
1. Advanced Site Management & Strategic Oversight
- Serve as the primary lead for high-complexity sites, conducting comprehensive monitoring visits (SQV, SIV, RMV, COV) with a focus on risk identification, strategic planning, and proactive issue resolution.
- Perform in-depth source data verification (SDV) and data trend analysis, utilizing advanced analytical skills to safeguard data integrity and patient safety.
- Drive site performance by developing and implementing tailored patient recruitment and retention strategies in partnership with investigators.
2. Mentorship, Training & Team Development
- Provide formal mentorship, coaching, and training to junior CRAs and site staff, elevating team capabilities and monitoring standards.
- Act as a subject matter expert (SME), contributing to the development of monitoring plans, study tools, and process improvements.
- Lead co-monitoring and assessment activities to ensure consistent quality and compliance across the monitoring team.
3. Cross-Functional Collaboration & Compliance Leadership
- Collaborate seamlessly with Clinical Operations, Data Management, and Safety teams to ensure aligned strategies and timely resolution of cross-functional challenges.
- Build and maintain senior-level, trust-based relationships with Principal Investigators and site coordinators, positioning ICON as a preferred partner.
- Champion regulatory compliance, ensuring all site activities adhere to ICH-GCP, local regulations, and ICON/sponsor SOPs. Represent monitoring during audits and inspections.
Who You Are: The Ideal Candidate
You are an accomplished, independent professional with a proven track record of excellence in clinical monitoring. You are a natural leader, a strategic thinker, and a dedicated mentor who thrives on driving results through expertise and influence.
Your Required Profile:
- Bachelor’s or advanced degree in Life Sciences, Nursing, Medicine, or a related field.
- Minimum of 5-8 years of experience as a Clinical Research Associate, with a demonstrated history of independently managing complex, multi-site clinical trials.
- Expert knowledge of ICH-GCP guidelines and major global regulatory requirements.
- Mastery of clinical trial software (EDC, CTMS, TMF) and advanced data review techniques.
- Proven leadership and mentorship abilities with experience guiding junior colleagues.
- Exceptional communication, negotiation, and stakeholder management skills.
- Ability and willingness to travel approximately 60% (domestic/international). A valid driver’s license is required.
What Sets You Apart:
- Experience in high-demand therapeutic areas (Oncology, Rare Diseases, Cell & Gene Therapy, Immunology).
- Professional certification (e.g., CCRA, SoCRA).
- Experience with Risk-Based Monitoring (RBM) and centralized monitoring practices.
- A track record of contributing to study-level documents and process improvement initiatives.
Why Advance Your Career as an SCRA at ICON?
1. Leadership Recognition & Strategic Impact
- Manage a portfolio of strategic importance with significant autonomy and direct visibility to study and senior leadership.
- Your expertise directly influences trial outcomes, client partnerships, and the professional growth of your peers.
2. Clear Pathway to Greater Influence
- This role is a recognized stepping stone to Lead CRA, Clinical Trial Manager (CTM), Site Management Lead, or Training/Quality roles.
- Play an integral part in shaping the standards and future direction of clinical monitoring at ICON.
3. Premier Senior Field Package
- Highly competitive salary and substantial performance-based bonus.
- Comprehensive travel and lifestyle package, including premium car allowance and full expense coverage.
- Enhanced annual leave and flexible benefits package.
- Premium health, wellness, and retirement programs for you and your family.
- Global Employee Assistance Programme and dedicated leadership development support.
Join a Culture that Values Your Expertise
At ICON, we believe that experienced professionals drive our success. We foster an inclusive environment where your knowledge is respected, your contributions are valued, and your career growth is actively supported.
Ready to leverage your expertise to lead sites, mentor colleagues, and shape the future of clinical development?
If you are a senior CRA seeking a role that matches your experience and leadership ambition, apply now.
