Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Site Monitor - Spain - FSP
Job ID R0000032229 , SpainDo 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 FSPis looking for aSite MonitorinSpain (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 3 yeras' experience in independent site monitoring - all types of visits and in oncology.
- 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
Send me your updated resume tomarta.kuniewicz@parexel.comfor an immediate interview.
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