At a Glance
- Tasks: Monitor clinical trials, ensuring compliance and quality across diverse sites.
- Company: TMC, a leader in rare diseases and oncology research.
- Benefits: Remote work with travel opportunities and a supportive team environment.
- Other info: Regular office visits in Hampshire; driving licence essential.
- Why this job: Make a real difference in groundbreaking clinical research while advancing your career.
- Qualifications: 4-5 years of monitoring experience and a life science degree required.
The predicted salary is between 46000 - 52000 £ per year.
Due to expansion, TMC are looking to hire a UK based experienced Senior CRA. As our specialisms are Rare and Orphan diseases and Oncology, experience in these areas is essential to the successful candidate.
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) E6 R3 and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (eTMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
- A minimum of 4-5 years of independent on-site monitoring.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree.
- Flexibility to travel to sites.
- A range of therapeutic area experience including oncology and rare and orphan diseases.
- Whilst the role is remote based, we will expect regular visits to the Head Office in Hartley Wintney, Hampshire.
- A driving licence is essential.
*Please note - this role is not eligible for UK visa sponsorship*
Senior Clinical Research Associate in Oxford employer: TMC Pharma Services Ltd
TMC is an exceptional employer for Senior Clinical Research Associates, offering a dynamic work culture that prioritises collaboration and innovation in the field of Rare and Orphan diseases and Oncology. With a strong commitment to employee growth, TMC provides ongoing training and development opportunities, alongside the flexibility of remote work complemented by regular engagement at our Head Office in Hartley Wintney, Hampshire. Join us to be part of a team that values your expertise and fosters a supportive environment for meaningful contributions to clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate in Oxford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those with experience in oncology and rare diseases. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We all know that knowledge is power, so make sure you can confidently discuss how you've applied these in your previous roles. It’ll show you're the right fit for the Senior CRA position.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and interests. Check out our website for openings at TMC and tailor your approach to highlight your experience in rare diseases and oncology. We want to see your passion!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Share a brief insight or question related to the interview discussion to show your enthusiasm and commitment to the role.
We think you need these skills to ace Senior Clinical Research Associate in Oxford
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in rare and orphan diseases and oncology. We want to see how your background aligns with our needs, so don’t be shy about showcasing relevant projects you've worked on!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the Senior CRA role. Share specific examples of your monitoring experience and how you’ve tackled challenges in previous studies.
Showcase Your GCP Knowledge:Since we’re all about Good Clinical Practice, make sure to mention your familiarity with GCP E6 R3 and ICH guidelines. We love candidates who can demonstrate their understanding of these standards in their application.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at TMC Pharma Services Ltd
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them in real-world scenarios.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past roles where you successfully managed clinical trial protocols. Highlight your experience with site monitoring visits and how you tackled challenges during those visits. This will demonstrate your hands-on expertise.
✨Demonstrate Flexibility and Communication Skills
Since the role involves regular communication with sites, be ready to discuss how you’ve effectively managed relationships in previous positions. Share instances where your flexibility helped adapt to changing project needs or recruitment plans.
✨Prepare Questions About the Role
Think of insightful questions to ask about the company’s approach to rare and orphan diseases and oncology. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.
