Offer summary

Qualifications:

Bachelor's degree in a life science or related discipline., Minimum of 3 years' experience in independent site monitoring and oncology., Understanding of ICH GCP Compliance., Excellent time management and social skills..

Key responsibilities:

Set up and oversee clinical study activities.

Complete study status reports and maintain documentation.

Participate in protocol and consent document submissions for ethics/IRB approval.

Assist in preparing regulatory submissions as needed.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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 Switzerland 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 years' experience in independent site monitoring 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 to marta.kuniewicz@parexel.com for an immediate interview.

Required profile