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Biomarker Consent Specialist

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Parexel

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Location:
United States

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

Not provided
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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

Additional Information:

Job Posted:
January 24, 2026

Work Type:
Remote work
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