Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
November 20
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
• Work independently and actively manage all necessary activities for setting up and monitoring a study. • Completing accurate study status reports and maintaining study documentation. • Dedicated to one sponsor, a global pharmaceutical company that leads the way in discovering and developing innovative health solutions.
• Bachelor's degree in a life science or related discipline. • At least 1 year of monitoring in the advertised country. • Essential - minimum of 1 year of active independent field monitoring experience as a CRA - all visits. • Deep understanding of ICH GCP Compliance. • Excellent time management and social skills. • Initiative-taking with a phenomenal eye for detail. • Ability to travel.
• Comprehensive benefits package including premium salary. • Car option. • Company cell phone and equipment. • Market leading PTO. • Culture of teamwork and collaboration. • Local line manager. • Excellent training. • People who motivate and face challenges together. • Innovative technology.
Apply NowOctober 9
10,000+
Conduct clinical monitoring and manage site compliance for trials at Thermo Fisher.