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- Tasks: Monitor clinical trial sites, ensuring compliance and quality in research practices.
- Company: IQVIA is a top global provider of clinical research services, driving healthcare innovation.
- Benefits: Enjoy flexible work options, career growth opportunities, and the chance to impact patient outcomes.
- Why this job: Be part of cutting-edge clinical trials and contribute to groundbreaking medical advancements.
- Qualifications: 2+ years of monitoring experience, preferably in Oncology, with a commitment to travel.
- Other info: This role is not eligible for UK Visa Sponsorship.
The predicted salary is between 30000 - 42000 £ per year.
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Join to apply for the Clinical Research Associate II role at IQVIA
Join Us on Our Mission to Drive Healthcare Forward
As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. We’re expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
Why IQVIA?
- IQVIA is recognized as #1 in its category on the 2025 Fortune World’s Most Admired Companies list for the FOURTH consecutive year!
- We offer genuine career development opportunities for those who want to grow as part of the organization.
- The chance to work on cutting edge medicines at the forefront of new medicines development.
- IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
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
Profile
- Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- Hands-on experience in the Oncology therapeutic area.
- Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Research, Analyst, and Information Technology
-
Industries
Pharmaceutical Manufacturing
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Clinical Research Associate II employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with current or former Clinical Research Associates at IQVIA or similar companies. Engaging with professionals in the field can provide you with insider knowledge about the role and the company culture, which can be invaluable during your application process.
✨Tip Number 3
Highlight your experience in managing multiple clinical trial protocols, especially in the Oncology therapeutic area. Be prepared to discuss specific examples of how you've successfully navigated challenges in previous roles, as this will set you apart from other candidates.
✨Tip Number 4
Prepare for questions related to site monitoring visits and how you handle communication with study sites. Being able to articulate your approach to building relationships and managing expectations will show that you're ready to take on the responsibilities of the role.
We think you need these skills to ace Clinical Research Associate II
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Clinical Research Associate II position at IQVIA. Understand the responsibilities and required qualifications, especially the emphasis on GCP compliance and oncology experience.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical trials, particularly any independent on-site monitoring roles you've held. Emphasise your familiarity with GCP and ICH guidelines, as well as your hands-on experience in the oncology therapeutic area.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for advancing clinical research and improving patient outcomes. Mention specific experiences that align with the responsibilities listed in the job description, such as managing multiple clinical trial protocols.
Proofread Your Application: Before submitting your application, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the role of a Clinical Research Associate.
How to prepare for a job interview at IQVIA
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Clinical Research Associate II. Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, as these will likely come up during your interview.
✨Showcase Your Experience
Be prepared to discuss your previous experience in clinical trials, especially any hands-on work in the Oncology therapeutic area. Highlight specific examples where you successfully managed multiple protocols or improved site performance.
✨Demonstrate Communication Skills
As a CRA, you'll need to establish regular lines of communication with sites. Be ready to provide examples of how you've effectively communicated with team members and site staff to manage expectations and resolve issues.
✨Ask Insightful Questions
Prepare thoughtful questions about IQVIA's approach to clinical research and their site management strategies. This shows your genuine interest in the company and the role, and it can help you assess if it's the right fit for you.
