Senior Clinical Research Associate

📋 Description

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify
• Handle appropriately sized clinical trials and support clinical study teams with larger scope trials
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities including

🎯 Requirements

• 4-year college degree or equivalent experience
• Holder of CRA certificate
• Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical
• Experience monitoring clinical trials across a variety of therapeutic areas
• Availability for domestic travel including overnight stays, which may constitute up to
• Fluency in English and the local language is required

🎁 Benefits

• Empowered to make an impact and build meaningful client relationships
• Opportunity to grow your career in an environment that values quality, accountability, and