At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Competitive salary, career growth, and a supportive learning environment.
- Other info: Flexible travel opportunities and a commitment to continuous learning.
- Why this job: Make a real impact on patient outcomes while working with innovative teams.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 40000 - 50000 £ per year.
Locations: Bath, United Kingdom; Reading, Berkshire, United Kingdom
Time type: Full time
Posted on: Posted Today
Job requisition id: R1540017
Join IQVIA on our mission to accelerate innovation for a healthier world!
IQVIA are seeking experienced Clinical Research Associates in South West England to strengthen our cFSP sponsor-dedicated team.
- We share a passion for the work we do, and the impact it has on customers and patients.
- We are innovative, curious, and feel empowered to explore new ideas and ways of working.
- We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise.
- We are committed to growth, always learning, and making the most of agile career opportunities.
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) 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 (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.
- 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.
Please note - this role is not eligible for UK visa sponsorship.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Senior CRA in Manchester employer: IQVIA LLC
At IQVIA, we pride ourselves on being a leading employer in the clinical research field, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through continuous learning opportunities and a supportive environment that encourages exploration of new ideas. Located in the picturesque South West of England, our team enjoys a fulfilling career while making a meaningful impact on patient outcomes worldwide.
StudySmarter Expert Advice🤫
We think this is how you could land Senior CRA in Manchester
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Understand their mission and values, especially how they relate to patient outcomes. This will help you tailor your answers and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your interview skills with a friend or mentor. Get comfortable discussing your experience with GCP and ICH guidelines, as well as your site monitoring visits. The more you practice, the more confident you'll feel when it’s time to shine!
✨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. So, get those applications in and let’s make an impact together!
We think you need these skills to ace Senior CRA in Manchester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior CRA role. Highlight your experience with site monitoring and knowledge of GCP and ICH guidelines. 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! Share your passion for clinical research and how you can contribute to our mission. Be genuine and let us know why you’re excited about this opportunity at IQVIA.
Showcase Your Experience:In your application, don’t just list your previous roles—describe your achievements! We love to see specific examples of how you've managed studies or improved processes. This helps us understand the impact you've made in your past positions.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re serious about joining our team!
How to prepare for a job interview at IQVIA LLC
✨Know Your GCP and ICH Guidelines
As a Senior Clinical Research Associate, it's crucial to have a solid grasp of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Brush up on these regulations before your interview, as you may be asked to discuss how you've applied them in past roles.
✨Showcase Your Monitoring Experience
Be prepared to share specific examples of your independent on-site monitoring experiences. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and ability to manage site relationships effectively.
✨Demonstrate Your Flexibility
Since the role requires travel to various sites, emphasise your flexibility and willingness to adapt to changing project needs. Share instances where you've successfully managed multiple priorities or adapted to new situations in your previous roles.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask thoughtful questions about the team dynamics, ongoing projects, or the company’s approach to innovation. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.
