Clinical Research Associate - Oncology - MD, VA or D.C. - FSP

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Clinical Research Associate - Oncology - MD, VA or D.C. - FSP
Primary Location: United States, Virginia, Remote Job ID R0000046752 Category Clinical Trials Date Posted 10/09/2026
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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
The Clinical Research Associate is responsible for the following:
Act as the primary site contact and site manager throughout all phases of a
clinical research study, taking overall responsibility of allocated sites
Key Accountabilities
Site Management Responsibilities
Supporting Activitiesmay include but not limited to the following
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial
Performs clinical study site management/monitoring activities in compliance with International Conference on Harmonization / Good Clinical Practices, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated Documents
Gains an in-depth understanding of the study protocol and related procedures
Coordinates and manages various tasks in collaboration with other sponsor roles to achieve Site Ready
Participates and provides inputs on site selection and validation activities
Performs remote and on-site monitoring & oversight activities using various tools to ensure:
Data generated at site are complete, accurate and unbiased
Subjects’ right, safety and well-being are protected
Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, closeout visits and records clear, comprehensive, and accurate visit & non-visit contact reports appropriately in a timely manner
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out
Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance
Identifies, assesses, and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with Clinical Research Manager and Partner Line Manager
Manages and maintains information and documentation in Clinical Trial Management System, electronic Trial Master File and various other systems as appropriate and per timelines
Team Development and Support
Contributes to CRA team knowledge by acting as process Subject Matter Expert, buddy/mentor and sharing best practices as appropriate/required
Supports and/or leads audits/inspection activities as needed
Performs co-monitoring visits where appropriate
Skills
Fluent in local languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
Hands on knowledge of Good Documentation Practices
Proven skills in Site Management including management of site performance and patient recruitment
Demonstrated high level of monitoring skill with independent professional judgement
Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices
Ability to understand and analyze data/metrics and act appropriately
Capable of managing complex issues, working solution-oriented manner
Performs root cause analysis and implements preventative and corrective action
Effective time management, organizational and interpersonal skills, conflict management, problem solving skills
Demonstrated high level of monitoring skill with independent professional judgement
Able to work highly independently across multiple protocols, sites, and therapy areas
High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment.
Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
Demonstrates commitment to Customer focus
Works with high quality and compliance mindset
Positive mindset, growth mindset, capable of working independently and being self-driven
Demonstrates and projects professional demeanor and communication consistent with organizational policies and practices
Ability to travel domestically and internationally approximately 65%-75% of working time
Expected travelling ~2-3 days/week
Current driver’s license required
Knowledge And Experience
Minimum 2 years of direct site monitoring experience in bio/pharma/CRO
Oncology monitoring experience required
Education
Bachelor’s degree preferred with a strong emphasis in science and /or biology
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
Watch Video
Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
Watch Video
Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
Watch Video
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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 Laurias: Manager, Clinical Operations
Laurias shares how Parexel has supported his career development from CRA to Clin Ops Manager and flexibility within the workplace.
Learn More

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