At a Glance
- Tasks: Oversee and monitor clinical trials, ensuring compliance and data quality.
- Company: Join a supportive and inclusive team at CellCentric.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to collaborate across teams and enhance your career.
- Why this job: Make a real impact in clinical research and contribute to innovative healthcare solutions.
- Qualifications: 10+ years of CRA experience and strong communication skills required.
The predicted salary is between 50000 - 65000 € per year.
The Sr. CRA is responsible for the oversight and monitoring of clinical trials to ensure they are conducted in compliance with the study protocol, ICH-GCP guidelines, applicable regulations, and company SOPs. The Sr. CRA provides CRO oversight or monitoring of site performance, data quality, patient safety, and timely trial execution through effective site management and communication. The Sr. CRA supports the Clinical Trial Manager in oversight of CRO.
This individual will contribute to the success of the team and organization by delivering on role-specific responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement.
Key Responsibilities- Site Management & Monitoring
- Conduct targeted oversight or monitoring activities for site selection, initiation, interim monitoring, and close-out visits
- Ensure trial conduct aligns with protocol, ICH-GCP, and regulatory requirements
- Oversee review and verify source data and ensure accurate, complete, and timely data entry
- Perform risk-based monitoring activities (remote and on-site as required)
- Training and escalation for CRO CRAs when necessary
- KPI and QTL review and updates to ensure the trial is operating at the highest quality
- Develop and review tools to support the monitoring or oversight of the CRO
- Proactively escalate to the CTMs/PD any deficiencies encountered in their daily work.
- Regulatory & Documentation
- Ensure essential documents are complete and filed appropriately (TMF/CIF/ISF)
- Support regulatory submissions and maintenance of site documentation
- Confirm proper informed consent processes are followed and documented
- Data Quality & Safety
- Identify and resolve data discrepancies with site staff and data management
- Support safety reporting processes (AEs/SAEs) and follow-up documentation
- Escalate quality issues and support CAPA implementation when needed
- Serve as primary point of contact for assigned sites, proactively address issues and provide solutions.
- Provide training and ongoing support to investigators and site teams
- Collaborate with cross-functional teams (Clinical Ops, DM, Safety, QA)
- Vendor and Study Support
- Coordinate with central labs, imaging, and other trial vendors as needed
- Track site performance metrics (enrolment, deviations, query resolution)
- Support study timelines and contribute to process improvements
- Oversight of CRA activities provided by third party
- Review CRO deliverables such as monitoring visit reports, follow-up letters, trip reports, and site communication for quality and completeness
- Track CRO performance using agreed metrics (e.g., monitoring visit timeliness, query aging, protocol deviation, TMF completeness)
- Escalate site and CRO issues as needed and contribute to issue management and resolution plans
- Participate and attend vendor meetings and have flexibility to support the team travelling abroad.
- Support oversight of TMF/eTMF completeness and filing practices, including CRO-generated documents
- Ensure CRO monitors are complying to risk-based monitoring plans and study-specific monitoring requirements
- Support audit/inspection readiness by ensuring CRO monitoring documentation and site files are inspection-ready
- Assist with review of CRO training compliance for assigned sites/staff
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field
- 10+ years of CRA or Clinical research experience
- Familiarity with ICH-GCP, UK/US/EU regulations, and clinical trial documentation
- Excellent organizational and time management skills
- Strong interpersonal and communication skills.
- Ability to work independently and manage multiple sites
- Ability to work across time zones
- Experience in Oncology preferably hematological cancers
- Proven ability to build trust and credibility through integrity, openness, and respect.
- Demonstrated accountability in delivering results and meeting commitments.
- Analytical mindset with the ability to use facts and data to guide decisions.
- Experience working on phase 2 and 3 registrational trials is preferred
- Trust and Respect: Act with integrity, honesty, and openness to build strong, credible relationships.
- Communication and Feedback: Share information clearly, listen actively, and engage in a culture of constructive feedback.
- Accountability and Reliability: Take ownership for performance, be dependable, and support others to achieve collective goals.
- Objectivity: Align on common objectives and use facts and data to reach fair, effective decisions.
- Team Balance and Enablement: Contribute to balanced roles within the team, support delegation, and help colleagues reach their full potential.
At CellCentric, we believe success is built on great teams. By embodying these working behaviors, every member contributes to a high-performing, supportive, and inclusive culture where individuals and the business thrive together.
Senior Clinical Research Associate (UK) Remote employer: CellCentric Limited
At CellCentric, we pride ourselves on fostering a collaborative and inclusive work environment that empowers our employees to excel in their roles. As a Senior Clinical Research Associate, you will benefit from our commitment to professional development, with ample opportunities for growth and advancement within the company. Our remote working model allows for flexibility while ensuring that you are part of a supportive team dedicated to making a meaningful impact in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate (UK) Remote
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their core values, especially around Trust and Respect, Communication, and Accountability. This will help you align your answers with what they’re looking for and show that you’re a great fit.
✨Tip Number 3
Practice your responses to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your answers, especially when discussing your experience in site management and monitoring.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can go a long way in showing your appreciation and keeping you top of mind. Plus, it’s a chance to reiterate your enthusiasm for the role.
We think you need these skills to ace Senior Clinical Research Associate (UK) Remote
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Clinical Research Associate role. Highlight your relevant experience, especially in clinical trials and compliance with ICH-GCP guidelines. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how you embody our core working behaviours like Trust and Respect. Let us know what makes you the perfect fit for our team.
Showcase Your Skills:Don’t forget to highlight your organisational and communication skills in your application. We value candidates who can manage multiple sites and work independently while maintaining strong relationships with site staff.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at CellCentric Limited
✨Know Your Protocols
Make sure you’re well-versed in ICH-GCP guidelines and the specific protocols relevant to the role. Brush up on your knowledge of clinical trial documentation and regulations, as this will show your commitment to compliance and quality.
✨Demonstrate Your Communication Skills
As a Senior Clinical Research Associate, effective communication is key. Prepare examples of how you've successfully managed site relationships or resolved issues in past roles. This will highlight your interpersonal skills and ability to work collaboratively.
✨Showcase Your Problem-Solving Abilities
Be ready to discuss specific challenges you've faced in previous trials and how you overcame them. This could involve data discrepancies or site performance issues. Demonstrating your analytical mindset will set you apart from other candidates.
✨Emphasise Teamwork and Accountability
Prepare to talk about how you’ve contributed to team success in past roles. Highlight instances where you took ownership of tasks or supported colleagues. This aligns with the core working behaviours of Trust and Respect, which are crucial for this position.
