Clinical Research Associate (CRA) - Oncology - US Any Region

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Clinical Research Associate (CRA) - Oncology - US Any Region
Primary Location: United States, Remote Job ID R0000046146 Category Clinical Trials Date Posted 09/21/2026
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Success profile
About this role
Potential career path
Employee insights
Our team
Why Clinical Research Associates work at Parexel
Learn about our culture
Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
Communicator
Detail-oriented
Flexible
Organized
Problem-solver
Self-starter
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About This Role
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
We are seeking a Clinical Research Associate (CRA) with oncology monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
You will conduct onsite monitoring activities, build and maintain productive site relationships, address site issues, and support enrollment and study delivery. Parexel provides world-class technology, training tailored to your experience, opportunities to work across therapeutic areas, and pathways for continued growth within clinical research.
Key Responsibilities
Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites, and prepare timely visit and contact reports.
Manage site quality and delivery from site identification through closeout.
Serve as the primary point of contact for assigned clinical sites, addressing questions and resolving issues to support successful study execution.
Oversee study integrity and build effective relationships with investigators and site staff.
Review trial performance at designated sites and help safeguard the rights, safety, and well-being of study participants in accordance with the protocol.
Develop patient recruitment strategies with clinical sites to support enrollment timelines.
Ensure compliance with approved standard operating procedures, study protocols and amendments, Good Clinical Practice, and applicable regulatory requirements.
Evaluate the quality and integrity of reported data, site performance, and investigational product accountability.
Monitor the completeness and quality of regulatory documentation and perform site document verification.
Candidate Profile
You'll Thrive In This Role If You Bring
Strong site relationship management, problem-solving, and communication skills.
The ability to work independently with urgency and limited oversight.
A client-focused, flexible approach to assignments and continuous learning.
The ability to manage multiple priorities, evaluate changing scenarios, apply study protocols, and meet project timelines.
An ethical, patient-focused approach and strong attention to quality and detail.
Comfort collaborating within a matrixed team and communicating clearly with internal and external stakeholders.
Required Qualifications
At least 18 months of direct onsite monitoring experience as a Clinical Research Associate.
Oncology clinical trial monitoring experience.
Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
Knowledge of Good Clinical Practice, applicable regulatory requirements, and clinical trial processes.
Experience using a Clinical Trial Management System, an Electronic Document Management System, and Microsoft Office applications, including Excel and Word.
Strong interpersonal, written, verbal, organizational, and problem-solving skills.
Benefits And Compensation
Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
For a complete list of benefits, please visit www.parexel.com/us-benefits (opens in new window).
Some roles may be eligible for additional incentives, bonuses, or other compensation programs. Our Talent Acquisition team will provide details on applicable bonus plans or incentive structures for eligible positions.
We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.
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!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
APEX CRA
CRA I
CRA II
Senior CRA
Project Management
Subject Matter Expert
People Management
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Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
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Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
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Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
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TEAM IMPRESSIONS
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Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
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Learn About Our Culture
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Meet Julie, a Senior Clinical Assistant, proud of her contribution
Julie welcomes volunteers at the Early Phase Clinic reception in

Work arrangement
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