Clinical Research Associate II
2 semanas atrás
At ICON, we are seeking a highly motivated and experienced Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for monitoring multiple Phase I, II, III, and IV clinical trial sites, across different therapeutic areas.
Key Responsibilities:
- Monitor multiple clinical trial sites, ensuring compliance with ICH/GCP guidelines
- Assist other CRAs with co-monitoring activities, both remote and on-site
- Collaborate with the team to develop commitment to study timelines and objectives
- Review source data to ensure patient safety and data integrity
- Escalate concerns/issues to other departments as appropriate
Requirements:
- Bachelor's Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry
- Minimum 12 months of independent Clinical Trials monitoring experience and site management experience
- Scientific background and proficiency with medical terminology
- Working knowledge of Local Regulations and ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
- Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits
- Fluent in English, both written and oral
- Strong technical skills with CTMS, eCRF, and eTMF
What We Offer:
- Competitive salary and benefits package
- Opportunities for professional growth and development
- Diverse and inclusive work environment
- Recognition and rewards for high performance
How to Apply:
Interested candidates should submit their application, including a cover letter and resume, to [insert contact information].
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