ATLAS MEDICAL SERVICES LTD. STI.
Site Care Partner (Oncology) - UK (Remote) - FSP
Get notified of more jobs like this · No spam, ever
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
My research opens up
new medical possibilities.
And I do it
Search Jobs
Keyword
Matching job links will appear below as you type.
Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures.
Radius: Enter distance 5 15 25 35 50
Unit MILES KM
View Remote Jobs View All Jobs
View remote jobs View all jobs
Site Care Partner (Oncology) - UK (Remote) - FSP
Primary Location: United Kingdom, Remote Job ID R0000046225 Category Clinical Trials Date Posted 09/23/2026
Apply Now
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
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 Site Care Partner to join our team in a remote capacity. This home-based position includes regular travel across the UK. As a Site Care Partner, you will serve as the primary point of contact for investigative sites throughout the clinical study lifecycle, supporting study start-up, activation, site engagement, recruitment performance, study conduct, and closeout activities.
This role plays a critical part in ensuring site operational success, patient safety, regulatory compliance, and high-quality study delivery. You will build and maintain trusted relationships with investigators and site personnel, coordinate with cross functional study teams, and help drive successful clinical trial execution from study initiation through completion.
You will join a collaborative and growth-oriented environment where your expertise directly contributes to advancing clinical research and helping bring new therapies to patients. This is an excellent opportunity to broaden your impact, strengthen strategic site partnerships, and further develop your career within a global clinical development organization.
Key Responsibilities
- Lead site start-up and activation activities, including site qualification, pre-trial assessments, site initiation activities, and activation readiness
- Support country and site selection processes by providing local intelligence, feasibility insights, and site assessment input
- Build and maintain strong relationships with investigator sites throughout the study lifecycle
- Serve as the operational point of contact for site level questions, coordinating issue resolution across study teams and stakeholders
- Ensure completion of required training, documentation, and systems activities necessary for successful site activation and study execution
- Drive site recruitment planning and enrolment support to help achieve study and country level targets
- Maintain regular communication with sites to monitor study progress, recruitment performance, and operational deliverables
- Review site monitoring reports and support site compliance with informed consent documentation and amendments
- Oversee site related deliverables, ensuring timely completion of data entry, data review activities, database lock readiness, and investigator documentation
- Proactively identify quality, compliance, and operational risks using study data and local intelligence, and implement appropriate mitigation plans
- Support implementation of decentralized trial capabilities and site adoption of study technologies and processes
- Collaborate with internal stakeholders to optimize communication, improve site experience, and strengthen study delivery outcomes
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Candidate Profile
You’ll Thrive In This Role If You Bring
- Strong relationship building, stakeholder management, and communication skills
- Experience working in clinical research and regulated healthcare environments
- The ability to collaborate effectively across cross functional and geographically diverse teams
- A patient focused mindset with strong attention to quality, compliance, and operational excellence
- Comfort working with clinical trial systems, study oversight processes, and site management activities
Required Qualifications
- Bachelor’s degree, Registered Nurse qualification, or equivalent combination of education, training, and experience
- At least 5 years of experience in clinical research, site management, monitoring, or a related field
- Demonstrated experience in site management with prior experience as a Site Monitor
- Demonstrated experience across the full clinical trial lifecycle, from study start-up and site activation through closeout
- Knowledge of ICH GCP, applicable regulatory requirements, and clinical trial processes
- Experience working with clinical trial systems such as EDC, Shared Investigator Platform, Site Profile, or similar clinical research technologies
- Strong communication, organizational, problem solving, and stakeholder management skills
- Ability to travel regularly throughout the UK, up to 50%
- Proficiency in English
Preferred Qualifications
- Experience supporting multinational clinical studies across a range of therapeutic areas
- Experience contributing to site feasibility, recruitment planning, and study performance optimization
- Familiarity with decentralized clinical trial capabilities and associated site technologies
- Subject matter expertise in clinical research systems, processes, or site management practices
Benefits And Compensation
- Medical & Dental Insurance
- Life Assurance
- Pension
- Critical Illness Insurance & Health Screenings
We offer a comprehensive benefits package to eligible employees, which includes life assurance, medical and dental insurance, and additional benefit offerings in accordance with the terms of our applicable plans.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
If this job does not sound like the next step in your career, but perhaps you know of someone who would 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.
Share this job
LinkedIn
Facebook
X
Email
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
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
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.
Learn About Our Culture
Meet David, a champion for disability inclusion
His leadership fosters workplace and clinical research inclusivity. Explore David's inspiring journey from combat medic to Parexel VP and Disability Inclusion Business Resource Group co-lead.
Learn More
Meet Marije, a Clinical Operations Manager in Parexel, is most proud of becoming a people leader
Marije, a former nurse and now Clinical Operations Manager in Parexel, is dedicated to enhancing patients' lives through her involvement in clinical research. Marije's exceptional leadership skills and impressive career growth further highlight her as a motivating individual.
Learn More
Meet Stacy Hurt, Chief Patient Officer at Parexel
Insights on Parexel's patient-centric approach, innovative strategies, and authentic culture in clinical research. Learn how Stacy's unique experiences shape the future of clinical trials.
Learn More
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
Meet Adriane, a Senior Clinical Operations Leader sharing insights and tips
Discover Adriane's role as a Clinical Operations Leader. She shares insights into her daily responsibilities, the skills crucial for success, and the rewarding challenges she faces. Learn how Parexel supported her career development and gain inspiration from her advice on professional growth.
Learn More
Clinical Operations Opportunities
Are you passionate about making a difference in the fight against cancer and beyond? At Parexel's
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Location