Clinical Research Associate II- Eye Care/Specialty/Aesthetics
New
United StatesFull-TimeMiddle
SalaryUSD 84500 - 162000 / year
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Job Details
- Experience
- Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials.
- Required Skills
- GCPCRM
Requirements
- Tertiary qualification in a health-related discipline (Medical, Scientific, Nursing).
- Minimum of 1 year of clinically related experience.
- Minimum of 6 months of experience in clinical research monitoring of investigational drug or device trials.
- Familiarity with risk-based, onsite, and offsite monitoring approaches.
- Advanced knowledge of local regulatory requirements, ICH/GCP Guidelines, and company policies.
- Strong interpersonal, communication, and presentation skills.
- Demonstrated ability to collaborate cross-functionally and manage competing priorities.
- Advanced ability to leverage technology and CRM tools for site engagement and tracking.
- Critical thinking and problem-solving skills to address site-specific issues.
Responsibilities
- Serve as the primary point of contact for investigative sites to strengthen partnerships.
- Train and motivate site staff and investigators on study protocols and clinical goals.
- Conduct site evaluation, training, monitoring, and closure activities in compliance with GCP, ICH, and AbbVie SOPs.
- Perform continuous risk assessment and collaborate with Central Monitoring to detect performance or safety issues.
- Manage investigator payments and ensure audit/regulatory readiness at assigned sites.
- Identify, evaluate, and recommend new potential investigators and research sites.
- Ensure high-quality data submission and timely follow-up for safety events.
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