Clinical Trial Coordinator

1 mese fa

Lombardia, Italia Buscojobs A tempo pieno

Clinical Trial Coordinator - Segrate, Milan

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.

Who is PPD Clinical Research Services?

PPD is a leading global contract research organization. Our purpose is to improve health. Our mission is to help customers deliver life-changing therapies. Our strategy is to bend the cost and time curve of drug development and optimize value for our customers. PPD is now part of Thermo Fisher Scientific. As the world leader in serving science, our Mission is to enable our customers to make the world healthier, cleaner and safer.

Clinical Trial Coordinator Responsibilities:

  • Provide technical support to the project team, coordinating non-clinical responsibilities of project administration.
  • Perform PPD investigator file reviews and log outstanding issues in project related tracking tools.
  • Review regulatory documents for proper content.
  • Liaise with monitor and investigative sites to resolve outstanding regulatory issues identified.
  • Disseminate study related information, including project tracking updates to clients, clinical study teams and other PPD departments.
  • Adhere to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.
  • Assist with the identification of potential investigators and development/distribution of initial protocol packets.
  • Create meeting agendas and minutes, as well as coordinate team conference calls and distribution of meeting minutes.

Education and Experience:

  • Master's degree (ideally within a clinical specialism), or equivalent education, training and experience.
  • Experience with submissions to Ethics Committees and Regulatory bodies (desired).
  • Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.
  • Experience managing multiple projects with differing priorities at one given time.
  • Exceptional communication, collaboration, organizational and time management skills.

What We Offer:

At PPD, we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly values a work-life balance.

Mission/4i Values:

Our Mission is to enable our customers to make the world healthier, cleaner and safer. 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 at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today

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