Contract Specialist/Sr Contract Specialist - FSP Dedicated

ThermoFisher Scientific; Deu; Hybrid; EUR 90,000 - 130,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Site Contract Specialist/Senior Contract Specialist to oversee contracts for clinical trials in a fast-paced FSP environment. You will draft, review, and negotiate agreements, ensuring compliance with local and international regulations, while coordinating with legal, clinical operations, regulatory affairs, and finance teams.

The role requires a Bachelor’s degree and extensive experience in contract management or negotiation within pharma or CRO settings,

Qualifications

• Bachelor’s degree in a relevant field (e.g., Law, Business) and strong experience in contract management.
• Experience negotiating high-value contracts in pharma or biotech settings.
• Excellent organizational and project-management skills with attention to detail.

Responsibilities

• Draft, review, and negotiate high-value contracts for clinical trials and related documents.
• Ensure regulatory compliance across local and international guidelines.
• Collaborate with legal, clinical operations, regulatory affairs, and finance teams.
• Mentor junior contract specialists and support team development.
• Manage contract lifecycle timelines and resolve issues promptly.

Skills

Contract management

Negotiation

Cross-functional collaboration

English proficiency

Education

Bachelor’s degree in a relevant field

Tools

Electronic contract management systems

Contract databases

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Site Contract Specialist - Make an Impact at the Forefront of Innovation

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. This opportunity is an exciting prospect for a big pharma company and for a new division focused on Oncology/Cell therapy

• 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.Support the resolution of contractual disputes and issues as they arise.Stay up-to-date with changes in regulations and industry standards related to clinical trial contracts.Mentor and provide guidance to junior contract specialists, assisting in their professional development.Participate in training sessions and workshops to enhance the contract management skills of the team. Qualifications: Bachelor’s degree in a relevant field (e.g., Law, Business Administration, Life Sciences).Extensive experience in contract management or negotiation within the pharmaceutical, clinical research, or related industry.Strong knowledge of contractual regulations and guidelines governing clinical trials.Excellent organizational and project management skills.Effective communication and interpersonal skills, with the ability to work collaboratively with cross-functional teams.Attention to detail and the ability to manage multiple projects and deadlines.Proficiency in both written and spoken English; additional language skills may be beneficial depending on the location. Preferred Qualifications: Advanced degree or certification in contract management or a related field.Experience in an FSP environment, providing services to multiple clients.Familiarity with electronic contract management systems and databases.Previous experience in a senior or leadership role within contract management.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.