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Parexel

End-to-end clinical trials and regulatory consulting

Contracts Manager - Clinical Research

Contract ManagementConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • Experience in contract management, proposal development, or a related field.
  • Knowledge of clinical trials and/or experience in the life sciences industry.
  • A university degree or equivalent experience.
  • Excellent negotiation skills.
  • Highly organized, with strong oral and written communication skills.
  • Good numeracy skills.
  • Excellent analytical and problem-solving skills.
  • Comprehensive knowledge of relevant software, including Windows, Word, Excel, Outlook, and databases.
  • Fluency in spoken and written English.

Responsibilities

  • Manage the contract process for specific or varied accounts, coordinating Operations, Project Management, Legal, Business Development, and Finance to prepare, review, and negotiate contracts.
  • Serve as the primary client contact during negotiations.
  • Maintain ongoing client communication regarding contractual issues throughout a project's lifetime.
  • Establish and maintain direct client contact.
  • Create, negotiate, and finalize budgets and contractual documents, including Start-up Agreements, Work Orders, and Change Orders.
  • Develop account-specific contract standards, including budget presentation, payment terms, and standard contract language, and discuss or negotiate them with clients as appropriate.
  • Proactively work with project management to review project status and contractual status, ensure compliance with contractual terms and milestones, and identify contract scope changes.
  • Work with Finance on ongoing budget changes and provide finance-system-load-ready budget tools in accordance with relevant policies and procedures.
  • Process information relating to contractual documents into relevant databases and maintain it there.
  • Customize company templates to meet client template requirements.
  • Participate in the development and testing of tools and procedures.

Desired Qualifications

  • Knowledge of ICH/GCP in the provision of clinical trials.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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