Clinical Research Associate (CRA) - Client-dedicated

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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.

Discover Impactful Work:

Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end 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 high-quality, cost-efficient clinical studies.

A day in the Life:

• Thrive in multi-national 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 life-sciences field

Experience

• Experience of independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation

Knowledge, Skills, Abilities

• 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 skill
• Fluency in Turkish and English languages