Parexel
• $110K — $130K *Qualifications
Responsibilities
Benefits
About the Role
Parexel is seeking a scientifically driven professional to support global clinical research programs by reviewing, interpreting, and negotiating genetic and biomarker informed consent language. You'll play a critical role in ensuring biospecimens and patient data are used in accordance with participant consent while partnering with leading pharmaceutical and biotech organizations.
This is a full-time, fully remote position and embedded within the partnership. Client team works EST hours. You will be working across all therapy areas.
What You'll Do
Review and interpret informed consent language for biospecimen and data use
Negotiate and manage genetic and biomarker consent requirements
Resolve complex consent and compliance questions with global stakeholders
Support high-impact clinical research and precision medicine initiatives
Required qualifications
Bachelor's degree in a scientific field
5+ years of experience with genetic and biomarker informed consents globally
Background in clinical trials, genetics, biomarkers, biobanking, or biospecimen management
Strong analytical, communication, and stakeholder management skills
Benefits and Compensation
Health, Vision and Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending and Health Savings Accounts
401(k) with Company match
Pet Insurance
If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!
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