Job Description: Clinical Research Associate (FSP)

Employment Type: Full-time Work Schedule: Standard (Monday-Friday) Environmental Conditions: Office

Position Overview

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.

The PPD FSP Solution

PPD's Functional Service Provider (FSP) division partners with and serves as an extension of our PPD team, supporting our customers' key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported, and technologically empowered to help customers manage capacity and set programs up for success. Joining within our PPD FSP functional area allows you to join the renowned PPD CRO and still gain invaluable client-dedicated experience.

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 services' mission is to improve health. 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 dedicated, forward-thinking, and upbeat teams.

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.

Keys to Success

Education

• University degree in a life-sciences field

Experience

• Minimum 6 months 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 skills
• Proficiency in both German and English languages is essential

Company Information

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.