Translational Medicine Scientist

Parexel; Columbus (OH); Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

FSA/HSA

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a scientifically driven professional to support global clinical research programs by reviewing, interpreting, and negotiating genetic and biomarker informed consent language. This full-time, fully remote role works with the partnership and EST hours across all therapy areas.

You will review consent language for biospecimen use, negotiate requirements, and resolve complex questions with global stakeholders to advance precision medicine initiatives.

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.

Responsibilities

• 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.

Skills

Analytical skills

Communication skills

Stakeholder management

Education

Bachelor's degree in a scientific field

Job description

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.

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

EEO Disclaimer

Parexel is an equal opportunity employer.

Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.