Jobs

CRA I - FSP - Central Scotland & North England


Job details
  • Thermo Fisher Scientific
  • 5 months ago

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

PPD's Functional Service Provider division partner with and serve 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.

Discover Impactful Work:

Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.

A day in the Life:

As a Clinical Research Associate, you will:

Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. Have excellent communication and interpersonal 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

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 Excellent command of German and English language
 

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

“Severely disabled applicants with the same aptitude will be given preferential treatment. / Schwerbehinderte Bewerber werden bei gleicher Eignung bevorzugt behandelt.”
 

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 

Sign up for our newsletter

The latest news, articles, and resources, sent to your inbox weekly.

Similar Jobs

CRA I/II - FSP

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...

Thermo Fisher Scientific

Analytical Chemist

Analytical Chemist - Pharmaceutical - Permanent - Craigoven - Shifts - Competitive Salary Plus Shift AllowanceWe are working with an exciting global pharmaceutical company that have ambitious growth plans and a clear vision for the future. The company that covers a range of services which includes clinical services, pharmaceutical development...

Seagoe

Analytical Technical Leader

Analytical Technical Leader – Pharmaceutical – Permanent – Craigoven – Days (Flexible Working)We are working with an exciting global pharmaceutical company that have ambitious growth plans and a clear vision for the future. The company that covers a range of services which includes clinical services, pharmaceutical development and API services...

Seagoe

Senior Analytical Chemist

Senior Analytical Chemist - Pharmaceutical - Permanent - Craigoven - Shifts - Competitive Salary Plus Shift AllowanceWe are working with an exciting global pharmaceutical company that have ambitious growth plans and a clear vision for the future. The company that covers a range of services which includes clinical services, pharmaceutical...

Seagoe

Clinical Research Associate 2

IQVIA UK are seeking Clinical Research Associates (CRA II ) to strengthen our cFSP team (sponsor dedicated).ResponsibilitiesPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesWork with sites...

Pharmiweb Reading

Validation Technical Leader (Computerised Systems Validation)

Validation Technical Leader (Computerised Systems Validation)Location: CraigavonHours:37.5Salary:CompetitiveBusiness Unit SciencesOpen To: Internal & External ApplicantsRef No.:HRJOB10245The RoleThe primary purpose of this role is to perform, and supervise staff in, activities within the validation lifecycle of all GMP systems requiring validation. This role is specifically in relation to Computerised Systems Validation (CSV)...

Almac Group Craigavon