Ofertes d'ocupació a Thermo Fisher Scientific

• Nivell d'experiència---
• Tipus de contracteA temps complert
• PublicadaNova

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Work Schedule

Standard (Mon-Fri)

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Office

Are you a student of a Master Degree in Clinical Research who would like to take his\her first steps within a dynamic clinical research organization? Are you interested in learning fundamental skills to start optimally your career?

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 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.

How will you make an impact?

The 6-month internship in Clinical Operations is designed to offer you the opportunity to develop insight into clinical research, master your skills while conducting meaningful work within the team. The program framework is crafted to allow you to grow professionally, learning invaluable skills to help you kick start your career!

What you will do?

As part of the Clinical Operations, you will work closely as a team, providing support and ideas for day to day activities. Your engagement and level of dedication will ensure that our project teams will receive the administrative and technical support they need. You will have a mentor who will help you navigate through our organization and processes and receive the best support, which will ensure you are on your way to reaching your goals.

You will be introduced to many diverse parts of the company and to other interns across Europe. You will have a wide portfolio of exciting tasks to complete. Plus test your natural curiosity in providing administrative and technical support to the team proactively, educating yourself about the clinical research industry and master your skills to measure your business progress.

How will you get here?

• You are undergoing a Master Degree in Clinical Research
• Having the ability to handle numerous tasks simultaneously
• Enjoying working in a team
• You also have excellent administration and organization skills and the ability to prioritize and time handle various tasks
• Passionate about common goals
• Demonstrate a positive demeanor and desire to succeed
• Exhibits a high degree of flexibility in adapting to a changing business environment
• English and Spanish proficiency
  
  

• Nivell d'experiència---
• Tipus de contracteA temps complert
• Publicada28 de gen.

Office

Work Schedule

Other

Environmental Conditions

Office

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.

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 execute high-quality, cost-efficient clinical studies.

As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract. Additional key responsibilities include:

• Performs investigator file reviews and logging of outstanding issues in project related tracking tools
• Reviews regulatory documents for proper content
• Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
• Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
• Assists with the identification of potential investigators and development/distribution of initial protocol packets
• Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
  
  

• University degree, or equivalent in education, training and experience
• Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
• Experience of manage multiple projects with differing priorities at one given time
• Exceptional communication, collaboration, organisational and time management skills
• Fluency in Spanish and English is essential