Clinical Research Associate - Ophthalmology & Biopharma
4 days ago
Description
• Utilize your skills to provide high standard of care for clinical trial participants • Responsible for all aspects of study site monitoring • Ensure proper materials are provided to study staff • Protect study patients by verifying informed consent procedures • Monitor data for missing or implausible data • Complete Serious Adverse Event (SAE) reporting • Assist with training of new employees and coordinate clinical projects
Requirements
• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) • 1-3 years of Clinical Monitoring experience • Ophthalmology experience is preferred but not required
Benefits
• Medical • Dental • Vision • Life • STD/LTD (multiple insurance carriers) • 401(K) • Paid time off (PTO) – Flex Plan • Employee recognition awards • Multiple ERG’s (employee resource groups)
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