Clinical Research Associate
Clinical Research Associate
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific youll 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 lifechanging 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.
Discover Impactful Work:
Our global Clinical Operations colleagues within our PPD clinical research services provide endtoend support for clinical trials from study start up to monitoring through to study close out across commercial and government contracts. Together we help clients define and develop clinical programs minimize delays and complete highquality costefficient clinical studies.
A day in the Life:
- Thrive in multinational project teams and be focused on delivering exemplary levels of customer service on multiple exciting 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.
Keys to Success:
Education
- University degree in a lifesciences field
Experience
- 1.5y Experience of independent onsite monitoring experience in a Pharmaceutical or Clinical Research Organisation
- Oncology experience
Knowledge Skills Abilities
- Demonstrated understanding of ICHGCP EU and FDA requirements
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Exceptional communication collaboration organisational and time management skill
- Fluency in Local language and English languages
Required Experience:
IC
Employment Type
Full-Time
