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Parexel Logo Parexel · Research and Development

Biomarker Consent Specialist

United States · Job Posted January 24, 2026
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Job Description

Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life- changing medicines to patients. As a Biomarker Consent Specialist, you’ll be joining a fast-paced, driven environment that’s helping to make life-changing differences to patients by negotiating, authoring, and reviewing genetic and biomarker language in clinical trial informed consents.

Job Responsibility

  • Author, review, and negotiate genetic and biomarker language within clinical trial informed consent documents
  • Document restrictions related to genetic and biomarker research on clinical trial samples
  • Understand and apply company policies and procedures to ensure consistency and compliance in informed consent language
  • Collaborate with global stakeholders to negotiate informed consents across multiple regions
  • Utilize clinical trial systems (eTMF, LIMS, etc.) to support documentation and workflow needs
  • Manage multiple concurrent assignments while meeting accelerated project timelines
  • Provide clear communication and partnership to cross‑functional teams to achieve study and organizational goals

Requirements

  • Exceptional communicator to partner effectively with internal and external teams
  • Self‑motivated professional who can work independently and collaboratively
  • Critical thinker able utilize and discern guidance documents as they apply to clinical trial informed consents
  • Proactive problem solver to identify issues, propose solutions, and drive resolution
  • Detail oriented individual with the ability to manage multiple assignments under accelerated timelines
  • Quick learner who can become proficient in client tools, databases, and systems
  • Proficient MS Office Suite user
  • Bachelor’s degree (BA/BS) required
  • Minimum of 5 years of experience working with global clinical trials and associated systems (eTMF, LIMS, or similar) AND proven experience with genetic informed consents and global consent negotiation

What we offer

  • Health, Vision & Dental Insurance
  • Tuition Reimbursement
  • Vacation/Holiday/Sick Time
  • Flexible Spending & Health Savings Accounts
  • Work/Life Balance
  • 401(k) with Company match
  • Pet Insurance
  • Flexible working hours
  • Professional growth and development opportunities
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