Clinical Operations Specialist
hace 4 semanas
About the Role
Parexel FSP is seeking a skilled Site Monitor to join our clinical operations team in Spain (Madrid or Barcelona). As a Site Monitor, you will work independently to set up and oversee studies, complete study status reports, and maintain study documentation.
Key Responsibilities
- Participate in the submission of protocols, consent documents for ethics/IRB approval, and assist in the preparation of regulatory submissions as requested.
- Work with world-class technology and training tailored to your individual experience.
- Collaborate with a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.
Requirements
- Bachelor's degree in a life science or related discipline.
- Minimum of 1.5 years' experience in independent site monitoring - all types of visits.
- Oncology experience.
- Understanding of ICH GCP Compliance.
- Excellent time management and social skills.
- Highly motivated with a phenomenal eye for detail.
- Ability to travel domestically and internationally approximately 65%-75% of working time.
- Current driver's license required.
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