At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Join IQVIA, a top-rated workplace recognised for innovation in healthcare.
- Benefits: Competitive salary, career growth, and a chance to make a real impact.
- Other info: Dynamic team environment with opportunities for continuous learning and development.
- Why this job: Be part of a mission to accelerate healthcare innovation and improve patient outcomes.
- Qualifications: 1 year of clinical research monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 € per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.
We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and #1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!). Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Essential Functions- 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) 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.
- 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.
- Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please note - this role is not eligible for UK visa sponsorship.
Research Associate in Chorlton cum Hardy employer: IQVIA
At IQVIA, we pride ourselves on being a top employer, recognised as a 2026 'Glassdoor Best Place to Work in the UK' and #1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list. Our collaborative work culture fosters continuous learning and professional growth, while our commitment to innovation in clinical research allows you to make a meaningful impact on global health outcomes. Join us in our mission to accelerate innovation for a healthier world and enjoy the unique advantages of working in a dynamic, supportive environment.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Chorlton cum Hardy
✨Tip Number 1
Network like a pro! Reach out to current or former employees at IQVIA on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research IQVIA’s projects and values. Show them you’re not just another candidate but someone who genuinely cares about their mission to improve health outcomes.
✨Tip Number 3
Practice makes perfect! Get a friend to do mock interviews with you. Focus on common questions for Clinical Research Associates and be ready to discuss your past experiences in detail.
✨Tip Number 4
Don’t forget to follow up! After your interview, send a thank-you email to express your appreciation for the opportunity. It shows you’re keen and professional, which can leave a lasting impression.
We think you need these skills to ace Research Associate in Chorlton cum Hardy
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your relevant experience, especially any site monitoring or clinical research work you've done. We want to see how your skills align with what we're looking for!
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 mission at IQVIA. Keep it concise but impactful – we love a good story!
Showcase Your Knowledge:Demonstrate your understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines in your application. We appreciate candidates who are well-versed in the regulatory landscape of clinical research.
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. Plus, it gives you a chance to explore more about our company culture and values.
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines before your interview. Being able to discuss these regulations confidently will show that you understand the core of clinical research and can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring experiences, especially those related to interventional studies. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will help illustrate your hands-on experience and problem-solving skills.
✨Showcase Your Communication Skills
Since the role involves liaising with various stakeholders, be ready to discuss how you've established effective communication lines in past projects. Share instances where you adapted your communication style to suit different audiences, whether they were site staff or team members.
✨Express Your Passion for Continuous Learning
IQVIA values individuals who are eager to learn and grow. Be prepared to talk about how you stay updated with industry trends and advancements. Mention any relevant courses, certifications, or conferences you've attended to demonstrate your commitment to professional development.
