When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
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 looking for a scientist to join our Translational Medicine team. This role will support our Sponsors in project management and operational execution for Digital Pathology. You will coordinate cross-functional activities related to whole-slide image transfer, vendor follow-up, request tracking, process documentation, and stakeholder communications. Working closely with scientific team members and vendors, you will ensure Digital Pathology workflows are organized, compliant, and executed on schedule.
Key Responsibilities
Coordinate cross-functional activities related to Digital Pathology operations
Manage whole-slide image transfer and tracking
Follow-up with vendors and manage vendor relationships
Track requests and maintain request management systems
Document processes and maintain compliance standards
Communicate with stakeholders across scientific and operational teams
Work Environment
Location: Rahway, NJ (onsite)
Hybrid: 2-3 days per week onsite preferred.
Schedule: Full-time
Required Qualifications
3+ years of experience in one or more of the following areas: Project Management, Clinical Trial Operations, Biomarker Operations, Lab Operations, Imaging, and Data Management
Experience with digital pathology
Experience in clinical trials
Bachelor's degree (BS or BA) in Life Sciences, Project Management, Clinical Operations, IT, Data Management, or related field
Strong organizational skills with experience tracking deliverables
Preferred Qualifications
Pharma/biotech industry experience
Experience with informed consent in clinical trials
Technical proficiency with:
Microsoft Lists
Power BI
SharePoint and Teams
AWS/S3-based workflows
LIMS (Laboratory Information Management System)
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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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.
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