Clinical Research Associate (Level I)
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.
Location / Division Specific Information
Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.
Discover Impactful Work :
PPD clinical research service s mission is to . It starts as an idea to cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people.
We invite you to re-imagine health promoting protocols with us, working alongside our .
A day in the Life :
Thrive in multi-national project teams and be passionate about delivering outstanding levels of customer service on multiple, ambitious projects.
- Have excellent communication and social skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
- Perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.
- Benefit from award winning training programmes that will assist your technical and professional skills and knowledge
Requirements :
- University degree in a life-sciences field
- Minimum 1+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
- Demonstrated understanding of ICH-GCP, EU and FDA requirements
- Demonstrated understanding of medical / therapeutic area knowledge and medical terminology
- Exceptional communication, collaboration, organisational and time management skills
- Fluent in German, English, French. Italian is a plus.
- Working permit and residence of Switzerland
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