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Thermo Fisher Scientific

Contract Specialist/Sr Contract Specialist

Thermo Fisher Scientific

. 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 .

Posted 11/3/2026full-timeRemote • GermanySeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating complex contracts for clinical trials, ensuring compliance with regulations and company policies. Proven ability to collaborate with cross-functional teams and mentor junior specialists while managing multiple projects effectively.

Highest-signal resume keywords
Contract ManagementClinical Trial Agreements (CTAs)Regulatory ComplianceProject ManagementNegotiation Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Contract DraftingContract NegotiationRegulatory GuidelinesAttention to DetailProject Management
Soft Skills
Effective CommunicationInterpersonal SkillsOrganizational SkillsCollaboration
Tools & Technologies
Electronic Contract Management SystemsDatabases
Certifications & Qualifications
Advanced Degree in Contract ManagementCertification in Contract Management
Industry Keywords
Clinical TrialsPharmaceutical IndustryClinical ResearchFSP Environment

About the role

Key responsibilities & impact
  • 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 comply with local and international regulations and company policies
  • Collaborate with legal, clinical operations, regulatory affairs, and finance teams
  • Liaise with clients, sites, and vendors to facilitate contract negotiation and approval
  • Monitor contract negotiations and address issues or concerns
  • Maintain accurate contract and agreement records and documentation
  • Provide contractual guidance and support to project teams throughout clinical trial lifecycles
  • Participate in developing and implementing contract management strategies and processes
  • Ensure timely contract execution to meet project timelines and deadlines
  • Support resolution of contractual disputes and issues
  • Stay current with clinical trial contract regulations and industry standards
  • Mentor and guide junior contract specialists
  • Participate in training sessions and workshops to enhance team contract management skills

Requirements

What you’ll need
  • 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
  • Advanced degree or certification in contract management or a related field (preferred)
  • Experience in an FSP environment, providing services to multiple clients (preferred)
  • Familiarity with electronic contract management systems and databases (preferred)
  • Previous experience in a senior or leadership role within contract management (preferred)