Clinical Research Associate

📋 Description

• Considered as the primary sponsor point of contact for investigative sites; provides contextual
• Aligns, trains, and motivates site staff and principal investigators on clinical trial program
• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure
• Understands site engagement and customizes site engagement strategies for assigned studies; gathers
• Connects study protocol, scientific principles, and clinical trial requirements to daily execution
• Develops solid knowledge of therapeutic area, asset, clinical landscape, and patient journey to

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (e.g., Medical, Scientific
• Independent clinical research monitoring experience of investigational drug or device trials in any
• Knowledge of appropriate therapeutic area indications and ability to understand and apply
• Knowledge of existing and emerging local regulatory and legal requirements, ICH/GCP guidelines, and
• Advanced communication skills and superior cross-functional collaboration skills among internal and
• Strong planning and organizational skills; ability to work effectively in a dynamic environment

🎁 Benefits

• Excellent development opportunities
• Reward and benefits package