At a Glance
- Tasks: Monitor clinical sites and ensure adherence to protocols for Oncology studies.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Gain valuable experience in a dynamic field with opportunities for growth.
- Other info: Flexible travel required; not eligible for visa sponsorship.
- Why this job: Make a real difference in healthcare while working on impactful studies.
- Qualifications: Life science degree or equivalent experience; knowledge of GCP and ICH guidelines.
The predicted salary is between 35000 - 45000 € per year.
Nottingham, United Kingdom | Full time | Field-based | R1514135
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.
*Please note - this role is not eligible for visa sponsorship*
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Clinical Research Associate in Nottingham 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 integrity and professional development, we provide a supportive environment where your contributions truly matter.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Nottingham
✨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 open doors to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. We recommend practising common interview questions and tailoring your answers to highlight your experience in oncology studies. Show them you’re the perfect fit!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We suggest mentioning something specific from your conversation to remind them of your enthusiasm and fit for the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Clinical Research Associate in Nottingham
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!
Be Honest and Clear:Remember, honesty is key in your application. Provide accurate information about your qualifications and experiences. We appreciate transparency and want to build a team we can trust!
Apply Through Our Website:To make sure your application gets noticed, apply directly through our website. It’s the best way for us to receive your details and keep track of your application. 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 protocols involved. Being able to discuss recent advancements or challenges in the field will show that you're not just familiar with the basics, but genuinely interested and engaged.
✨Master Good Clinical Practice (GCP)
Since GCP is a big 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. Highlighting your ability to manage expectations and resolve issues will be key.
✨Prepare for Site Monitoring Scenarios
Think about potential scenarios you might face during site monitoring visits. Prepare to discuss how you would handle recruitment challenges or quality issues at a site. This will showcase your problem-solving skills and readiness for the role.
