At a Glance
- Tasks: Coordinate clinical trials and ensure compliance with regulations in a dynamic research environment.
- Company: Join The Royal Marsden NHS Foundation Trust, a leader in cancer research.
- Benefits: Competitive salary, inclusive workplace, and opportunities for professional growth.
- Other info: Flexible working across sites and commitment to diversity and inclusion.
- Why this job: Make a real difference in cancer research while developing your career.
- Qualifications: Experience in clinical trials and a relevant degree or equivalent experience.
The predicted salary is between 37338 - 44962 € per year.
An exciting opportunity has arisen for a Senior Clinical Trial Administrator to join the Breast Clinical Research Unit at The Royal Marsden NHS Foundation Trust, based at both our Sutton and Chelsea sites.
Main duties of the job:
- Take responsibility for ensuring clinical trials within the unit are conducted and managed in accordance with Good Clinical Practice and Trust SOPs.
- Be responsible for conveying the requirements of the Clinical R&D Office to clinical staff within their allocated Clinical Unit.
- Provide an efficient clinical trial coordination service to the unit, ensuring trials fulfil all statutory requirements.
- Oversee the conduct of trials within the unit and maintain day to day responsibility for specific trials within the Unit.
- Represent the unit at key meetings and deputise for the Research Operations Manager as required.
Detailed job description and main responsibilities:
- Ensure all research within the unit receives all relevant regulatory approval before it commences.
- Implement systems within the unit to ensure research cannot commence without all regulatory approvals.
- Under the direction of the Research Operations Manager, lead implementation of systems within the unit to ensure all clinical trials are conducted in accordance with all regulatory requirements including:
- Medicines for Human Use (Clinical Trials) Regulations
- Research Governance Framework for Health and Social Care
- Human Tissue Act
- Review capacity and resource requirements within the unit for coordination and administrative management of trial portfolio and advise the Research Operations Manager accordingly.
- Ensure all patients consented to clinical trials in the unit are recorded on the electronic patient record (EPIC).
Person specification:
Education/Qualifications:
- Recent GCP training
- Life Sciences (or equivalent) degree or relevant experience
Experience:
- Demonstrable experience of working in a clinical trial setting
- Understanding of clinical trials and regulations governing clinical research
- Experience of working in the NHS or equivalent
- Experience of working in the field of oncology
Skills Abilities/knowledge:
- Excellent administrative and organisational skills
- Experience of data entry and data management
- Excellent oral and written communication skills
- Ability to interact with, influence and motivate people at all levels
- Ability to interact confidently with experts and non-experts
- Ability to maintain adherence to written procedures
- Experience of supervising administrative staff
Other Requirements:
- Able to work on both sites and to be flexible to meet the needs of the role
The Royal Marsden values diversity and is committed to the recruitment and retention of underrepresented minority groups. We particularly welcome applications from Black, Asian and minority ethnic candidates, LGBTQ+ candidates and candidates with disabilities. We are a Disability Confident Employer and are committed to creating an inclusive workplace that enables staff to reach their full potential.
Senior Clinical Trial Coordinator employer: Royal Marsden
The Royal Marsden NHS Foundation Trust is an exceptional employer, offering a dynamic work environment within the Breast Clinical Research Unit at our Sutton and Chelsea sites. We pride ourselves on fostering a culture of inclusivity and professional growth, providing employees with opportunities to develop their skills in clinical research while contributing to groundbreaking oncology trials. Our commitment to diversity and support for underrepresented groups ensures that all staff can thrive and make a meaningful impact in their roles.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Trial Coordinator
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at The Royal Marsden or similar institutions. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice and the specific regulations mentioned in the job description. We want you to be able to discuss how your experience aligns with their needs confidently!
✨Tip Number 3
Showcase your organisational skills during the interview. Bring examples of how you've successfully managed clinical trials or coordinated teams in the past. This will help us see that you're the right fit for the Senior Clinical Trial Coordinator role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team at The Royal Marsden.
We think you need these skills to ace Senior Clinical Trial Coordinator
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Clinical Trial Coordinator role. Highlight your relevant experience in clinical trials, especially any work with Good Clinical Practice and NHS regulations. We want to see how your background fits perfectly with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills align with our needs at The Royal Marsden. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Skills:Don’t forget to highlight your excellent administrative and organisational skills in your application. Mention any experience you have with data management and your ability to communicate effectively with both experts and non-experts. We’re looking for someone who can motivate and influence others!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role and our values there!
How to prepare for a job interview at Royal Marsden
✨Know Your Regulations
Make sure you brush up on the Medicines for Human Use (Clinical Trials) Regulations and the Research Governance Framework. Being able to discuss these regulations confidently will show that you understand the legal landscape of clinical trials, which is crucial for the role.
✨Showcase Your Experience
Prepare specific examples from your past work in clinical trials, especially in oncology if possible. Highlight your experience with Good Clinical Practice and how you've ensured compliance in previous roles. This will demonstrate your hands-on knowledge and ability to manage trials effectively.
✨Communication is Key
Since you'll be interacting with various stakeholders, practice articulating complex information clearly. Think about how you can explain trial processes to both experts and non-experts. This skill is vital for conveying requirements to clinical staff and ensuring everyone is on the same page.
✨Be Ready to Lead
As a Senior Clinical Trial Coordinator, you'll need to show leadership qualities. Prepare to discuss how you've led teams or projects in the past, particularly in coordinating trials. Emphasise your ability to motivate others and maintain adherence to procedures, as this will be a key part of your role.
