Thermo Fisher Scientific logo
Thermo Fisher Scientific

The World Leader In Serving Science

Contract Specialist, Senior Contract Specialist - FSP Dedicated

Contract SpecialistGeneralFull TimeRemoteSeniorTeam 10,001+Since 1956H1B SponsorCompany SiteLinkedIn

Location

Bulgaria

Posted

1 day ago

Salary

0

Seniority

Senior

Bachelor DegreeEnglish

Job Description

Contract Specialist, Senior Contract Specialist - FSP Dedicated

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. • 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.

Job Requirements

  • 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.

Benefits

  • Health insurance
  • Flexible work arrangements
  • Professional development opportunities

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