At a Glance
- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, make an impact, and enjoy continuous learning.
- Other info: Flexible travel required; great opportunity for career growth.
- Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 € per year.
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. Apply today and forge a career with greater purpose, make an impact and never stop learning!
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.
Research Associate in Hucknall employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters continuous learning and professional growth. As a Clinical Research Associate, you will play a vital role in advancing oncology studies across the UK, supported by a collaborative team dedicated to making a meaningful impact on global health. With a commitment to integrity and innovation, we provide our employees with the tools and opportunities to thrive in their careers while contributing to a healthier world.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Hucknall
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by researching IQVIA's recent projects and values. Show us that you're not just another candidate; you’re genuinely interested in making a difference in the healthcare world.
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. We want to see your personality shine through, so don’t be afraid to let your passion for oncology and research come across!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen. Plus, it shows us you’re proactive and really keen on joining our mission to create a healthier world.
We think you need these skills to ace Research Associate in Hucknall
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in site monitoring and any relevant oncology studies you've worked on. We want to see how your background aligns with 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 you can contribute to our team. Keep it engaging and personal – we love to see your personality come through.
Showcase Your GCP Knowledge:Since Good Clinical Practice is key in this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for candidates who can ensure compliance and maintain high standards in their work.
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 to join our team at IQVIA!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies. Familiarise yourself with the latest trends and challenges in this area, as well as the specific protocols and regulations that govern clinical trials. This will show your potential employer that you're not just interested in the role, but that you’re genuinely passionate about making a difference in this field.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the job, ensure you can discuss it confidently. Review the guidelines and be prepared to explain how you've applied them in past experiences. Being able to demonstrate your understanding of these principles will set you apart from other candidates.
✨Prepare for Site Management Scenarios
Think about potential scenarios you might face while monitoring sites. Prepare examples from your past experience where you successfully managed site issues or improved recruitment strategies. This will help you illustrate your problem-solving skills and adaptability during the interview.
✨Show Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Be ready to discuss how you’ve effectively communicated with sites and team members in the past. Highlight any experience you have in training or mentoring others, as this will demonstrate your ability to establish strong working relationships.
