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- Tasks: Join a dynamic team as a Clinical Research Associate, managing clinical monitoring across exciting projects.
- Company: Thermo Fisher Scientific is a global leader in making the world healthier, cleaner, and safer.
- Benefits: Enjoy competitive pay, annual bonuses, healthcare, and a commitment to diversity and inclusion.
- Why this job: Make a real impact on global health while developing your skills in a supportive environment.
- Qualifications: A university degree in life sciences and at least 6 months of relevant experience required.
- Other info: Join a team of over 100,000 colleagues dedicated to integrity, innovation, and career growth.
The predicted salary is between 28800 - 42000 £ per year.
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 resources to achieve individual career goals while advancing science through research, development, and delivery of life-changing therapies. Our work spans laboratory, digital, and decentralized clinical trial services, with clinical trials conducted in over 100 countries. Your dedication to quality and accuracy will help improve health outcomes for communities worldwide.
PPD's Functional Service Provider division supports our clients' key functions, covering needs at all levels with a commitment to quality. We deploy top-tier talent in all engagement models, supported by rigorous training and technological empowerment to help manage capacity and set programs up for success. Joining our PPD FSP team offers client-dedicated experience within the renowned PPD CRO environment.
A day in the Life
- Work within multinational project teams, delivering high levels of customer service across multiple projects.
- Exhibit excellent communication and interpersonal skills, taking ownership of your work in a collaborative environment.
- Perform and coordinate all aspects of clinical monitoring, with the qualification to conduct activities independently.
- Benefit from award-winning training programs to enhance your technical and professional skills.
Keys to Success
- Education: University degree in a life sciences field.
- Experience: At least 6 months of independent, on-site monitoring experience in a pharmaceutical or CRO setting.
- Knowledge, Skills, Abilities: Understanding of ICH-GCP, EU, and FDA requirements. Knowledge of medical/therapeutic areas and medical terminology. Strong communication, collaboration, organizational, and time management skills. Excellent command of English.
Benefits
We offer competitive pay, annual bonuses, healthcare, and various employee benefits. Join an organization committed to integrity, innovation, and career development. Our culture values diversity and inclusion. Severely disabled applicants with the same aptitude will be given preferential treatment. Our Mission is to enable our customers to make the world healthier, cleaner, and safer.
Join our team of over 100,000 colleagues sharing values of Integrity, Intensity, Innovation, and Involvement. Apply today at http://jobs.thermofisher.com. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and provides accommodations for applicants with disabilities. For assistance, contact 1-855-471-2255.
Contact Detail:
Thermo Fisher Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA I/II - FSP - UK
✨Tip Number 1
Familiarise yourself with ICH-GCP, EU, and FDA requirements. Understanding these regulations is crucial for a Clinical Research Associate role, and demonstrating your knowledge during interviews can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry events or join relevant online forums to connect with current employees at Thermo Fisher Scientific. This can provide you with insider insights and potentially a referral.
✨Tip Number 3
Highlight your independent monitoring experience. Be prepared to discuss specific projects where you took ownership and delivered results, as this will demonstrate your capability to work autonomously in a collaborative environment.
✨Tip Number 4
Showcase your communication and organisational skills. Prepare examples of how you've effectively communicated within teams and managed multiple tasks, as these are key attributes for success in the CRA role.
We think you need these skills to ace CRA I/II - FSP - UK
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the CRA I/II position at Thermo Fisher Scientific. Familiarise yourself with the key skills needed, such as knowledge of ICH-GCP and experience in clinical monitoring.
Tailor Your CV: Customise your CV to highlight relevant experience, particularly any independent, on-site monitoring experience in a pharmaceutical or CRO setting. Emphasise your educational background in life sciences and any specific skills that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the company’s mission. Mention how your skills and experiences make you a great fit for the team and how you can contribute to making the world healthier, cleaner, and safer.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is accurate and presented professionally. A polished application reflects your attention to detail, which is crucial for a Clinical Research Associate.
How to prepare for a job interview at Thermo Fisher Scientific
✨Understand the Role
Make sure you have a solid grasp of what a Clinical Research Associate does, especially in the context of Thermo Fisher Scientific. Familiarise yourself with their mission and how your role contributes to making the world healthier, cleaner, and safer.
✨Showcase Your Experience
Be prepared to discuss your previous monitoring experience in detail. Highlight specific projects where you took ownership and delivered results, as this will demonstrate your capability to work independently and collaboratively.
✨Know the Regulations
Brush up on ICH-GCP, EU, and FDA requirements. Being able to discuss these regulations confidently will show that you are knowledgeable and serious about compliance, which is crucial in clinical research.
✨Demonstrate Communication Skills
Since excellent communication is key for this role, practice articulating your thoughts clearly and concisely. Prepare examples of how you've effectively communicated within teams or with clients in past roles.
