Clinical Operations Specialist

hace 4 semanas


Alcobendas, Madrid, España Parexel A tiempo completo
Parexel FSP: A Leader in Clinical Operations

Why Choose Us?

We are one of only three CROs to have received the Leadership Award for 11 consecutive years. Our team's 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.

About the Role

We are seeking a Site Monitor in Spain (Madrid or Barcelona) to strengthen our clinical operations team. As a Site Monitor, you will work independently and be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation.

Key Responsibilities
  • Participate in the submission of protocols, consent documents for ethics/IRB approval
  • Assist in the preparation of regulatory submissions as requested
  • Work 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
What We Offer

Long-term projects, world-class technology, and training tailored to your individual experience. Work from home and with the flexibility you want. Our SMs have less travel and less workload to maintain work-life balance.



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