Contract Specialist/Sr Contract Specialist - FSP Dedicated - EMEA

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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 team is expanding, and we are looking to recruit a Contract Specialist or Senior Contract Specialist for our growing FSP environment.

• The Contract Specialist in the FSP group is responsible for managing and overseeing contractual aspects of clinical trials conducted by the FSP on behalf of its clients. This role involves negotiating, drafting, and finalizing high-value and complex contracts, ensuring compliance with relevant regulations, and maintaining effective communication with internal and external stakeholders. The Senior Contract Specialist also provides mentorship and guidance to junior contract specialists.
   

  Key Responsibilities:

  • Draft, review, and negotiate high-value and complex contracts related to clinical trials, including Clinical Trial Agreements (CTAs), Confidentiality Agreements (CDAs), and other relevant documents.
  • Ensure contracts are compliant with local and international regulations and company policies.
  • Collaborate with internal teams, including legal, clinical operations, regulatory affairs, and finance, to ensure alignment and compliance with contractual requirements.
  • Liaise with external stakeholders, including clients, sites, and vendors, to facilitate the contract negotiation and approval process.
  • Monitor the progress of contract negotiations and address any issues or concerns that arise.
  • Maintain accurate records and documentation related to contracts and agreements.
  • Provide guidance and support to project teams on contractual matters throughout the lifecycle of clinical trials.
  • Participate in the development and implementation of contract management strategies and processes.
  • Ensure timely execution of contracts to meet project timelines and deadlines.