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.
Skills Required
- 3+ years of experience in project management, clinical trial operations, biomarker operations, lab operations, imaging, or data management
- Experience with digital pathology
- Experience in clinical trials
- Bachelor's degree in life sciences, project management, clinical operations, IT, data management, or a related field
- Strong organizational skills and experience tracking deliverables
- Pharma or biotechnology industry experience
- Experience with informed consent in clinical trials
- Technical proficiency with Microsoft Lists, Power BI, SharePoint, Teams, AWS or S3-based workflows, and LIMS
Parexel Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.
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Healthcare Strength — Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
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Retirement Support — Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
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Leave & Time Off Breadth — Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.
Parexel Insights
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
