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Contract Specialist, Senior Contract Specialist
Thermo Fisher ScientificContract Specialist managing clinical trial contracts for a pharma company. Involving negotiation and oversight of high-value agreements in a growing FSP environment.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in drafting, reviewing, and negotiating complex contracts for clinical trials, ensuring compliance with regulations and company policies. Proficient in contract management strategies and capable of mentoring junior specialists while collaborating effectively with cross-functional teams.
Highest-signal resume keywords
Contract ManagementClinical Trial Agreements (CTAs)Regulatory ComplianceNegotiation SkillsProject Management
ATS Keywords
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Hard Skills
Contract DraftingContract ReviewContract NegotiationRegulatory GuidelinesClinical Trial RegulationsDocumentation ManagementContractual Dispute ResolutionContract Management StrategiesAttention to DetailProject Execution
Soft Skills
Effective CommunicationInterpersonal SkillsOrganizational SkillsCollaborationMentoring
Industry Keywords
Clinical TrialsPharmaceutical IndustryClinical ResearchConfidentiality Agreements (CDAs)Stakeholder LiaisonCross-Functional TeamsProject TimelinesProfessional DevelopmentTraining SessionsWorkshops
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 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.
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.
Benefits
Comp & perks- Professional development opportunities
- Flexible working arrangements