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 flexibility, competitive salary, and opportunities for professional growth.
- Other info: Regular travel to the Head Office required; driving licence essential.
- Why this job: Join a dynamic team making a real difference in healthcare.
- Qualifications: 4-5 years of monitoring experience and knowledge of GCP/ICH guidelines.
The predicted salary is between 45000 - 55000 £ 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 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 fields 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
✨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 being knowledgeable is key, so make sure you can discuss how you've applied these in your previous roles. Confidence is everything!
✨Tip Number 3
Showcase your site management skills! During interviews, share specific examples of how you've successfully managed multiple clinical trials. This will demonstrate your ability to handle the responsibilities of a Senior CRA.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in oncology and rare diseases. We want to see how your background aligns with our needs, so don’t be shy about showcasing relevant projects and achievements!
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 make you the perfect fit for the Senior CRA role. Keep it engaging and personal!
Showcase Your Monitoring Experience:Since we’re looking for someone with solid on-site monitoring experience, be sure to detail your past roles and responsibilities. Highlight specific trials you've managed and any challenges you've overcome.
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’s super easy!
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 before the interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you truly understand their importance in clinical research.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully managed clinical trials, especially in oncology or rare diseases. Highlight how you adapted recruitment plans or resolved issues at sites, as this will demonstrate your hands-on experience and problem-solving skills.
✨Communicate Effectively
Since the role involves regular communication with study sites, practice articulating your thoughts clearly and concisely. You might even want to role-play common scenarios with a friend to ensure you can handle questions about managing site expectations and quality issues smoothly.
✨Be Ready to Discuss Travel Flexibility
As the position requires travel to various sites, be prepared to discuss your flexibility and willingness to travel. It’s also a good idea to mention any previous experiences you have had with site visits and how you managed your time effectively while on the road.
