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.