Remote Senior Clinical Research Associate

Summary

Join the company that focuses on its people and invests in their professional development and success.

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in South Africa
• Experience in all types of monitoring visits in Phase II and/or III
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration and problem-solving skills
• Ability to travel and a valid driver’s license

Responsibilities

• Conduct and report all types of onsite monitoring visits as well as remote visits
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be involved in site identification process
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions