At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in oncology research.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Full-time role with travel opportunities and professional growth.
- Other info: Dynamic field-based role with a focus on collaboration and communication.
- Why this job: Make a real difference in cancer research while gaining valuable experience.
- Qualifications: Experience in oncology monitoring and knowledge of GCP guidelines required.
The predicted salary is between 35000 - 45000 € per year.
Chesterfield, United Kingdom | Full time | Field-based
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK.
Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- 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 (TMF) 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:
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Clinical Research Associate in Chesterfield employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. Our commitment to employee growth is evident through comprehensive training programmes and opportunities to work on impactful Oncology studies across the UK, all while contributing to our mission of creating a healthier world. With a focus on flexibility and support, we ensure our Clinical Research Associates thrive in their roles, making a meaningful difference in the lives of patients.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Chesterfield
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios specific to Clinical Research Associates. We recommend role-playing with a friend or using mock interview platforms to boost your confidence.
✨Tip Number 3
Showcase your skills during interviews by sharing relevant experiences from your past roles. We love hearing about how you’ve tackled challenges in site monitoring or improved recruitment strategies!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive roles listed there that you won’t find anywhere else.
We think you need these skills to ace Clinical Research Associate in Chesterfield
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you fit into our mission!
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 background aligns with our goals at StudySmarter. Keep it engaging and personal!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We love seeing candidates who are well-versed in these areas!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies and the specific challenges they present. Being able to discuss recent advancements or common issues in this field will show that you're not just familiar with the basics, but that you're genuinely interested and engaged.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the role, ensure you can confidently discuss its principles and how they apply to site monitoring. Prepare examples from your past experiences where you adhered to these guidelines, as this will demonstrate your commitment to quality and compliance.
✨Show Off Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Be ready to share examples of how you've effectively communicated with sites or team members in the past. Highlight any strategies you've used to resolve conflicts or manage expectations.
✨Prepare for Site Monitoring Scenarios
Think about potential scenarios you might face during site visits and how you would handle them. This could include recruitment challenges or quality issues. Practising your responses will help you feel more confident and articulate during the interview.
