Spain Job Openings
Parexel
Site Monitor - Oncology - Spain - FSP
October 17, 2024
Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do.
Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people.
Parexel FSP is looking for a Site Monitor in Spain (Madrid or Barcelona) to strengthen our clinical operations team. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience.
As a SM, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.
You will possess:
#LI-REMOTE
Join our team and develop your career with us by contributing your personal and professional talents and skills. Together we will continue to do things that matter to people.
Parexel FSP is looking for a Site Monitor in Spain (Madrid or Barcelona) to strengthen our clinical operations team. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance. We offer long-term projects, world-class technology and training tailored to your individual experience.
As a SM, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
You will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.
You will possess:
- Bachelor's degree in a life science or related discipline.
- Minimum of 1,5 yeras' 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. Expected travelling ~2-3 days/week
- Current driver’s license required
#LI-REMOTE
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