Clinical Research Associate I

Position Summary:

• Seasoned, experienced professional in monitoring and site management.
• Responsibilities include activities involving start-up and study implementation, on-site monitoring and site management.
• Works independently as a study team member.

Essential Functions:

• Oversees all aspects of study site management.
• Updates, tracks and maintains study specific trial management tools/systems, and status reports.
• Prepares and submits accurate and timely monitoring reports from all site visits.

Qualifications:

• University degree life science/pharmacy/other health related discipline or equivalent experience.
• Excellent communication and organizational skills are essential.
• Ability to travel overnight, up to 60% on average. International travel as needed.