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- Tasks: Join our team as a Clinical Research Associate, performing site monitoring visits and managing study progress.
- Company: IQVIA is a global leader in clinical research, driving healthcare innovation and improving patient outcomes.
- Benefits: Enjoy career development opportunities, consistent workload, and cutting-edge tools like an iPad for efficiency.
- Why this job: Be part of groundbreaking medicine development and work with significant data to enhance site performance.
- Qualifications: A life science degree and independent on-site monitoring experience are essential; flexibility and strong communication skills are a must.
- Other info: This role is not eligible for UK visa sponsorship.
The predicted salary is between 36000 - 60000 £ per year.
Our Sponsor Dedicated (cFSP) team is growing and we are looking for aspiring CRAs of all levels, join us on our mission to drive healthcare forward!
What We Offer / USPs
- 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!
- We offer genuine career development opportunities for those who want to grow as part of the organization.
- We invest in keeping our teams stable, so workload is consistent.
- As a CRA you will receive an iPad and use of key developments such as site visit apps, site visit report apps that allow CRAs to do their day job more efficiently.
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.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Requirements
- You should be life science degree educated.
- You have experience of independent on-site monitoring experience.
- You've handled multiple protocols and sites across a variety of drug indications.
- Flexibility and ability to travel.
- Strong communication, written and presentation skills.
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
Experienced Clinical Research Associate, Sponsor Dedicated employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate, Sponsor Dedicated
✨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 Clinical Research Associates or professionals in the field. Engaging with them can provide insights into the role and the company culture, which can be invaluable during your application process.
✨Tip Number 3
Stay updated on the latest trends and advancements in clinical research. Being knowledgeable about cutting-edge medicines and technologies can set you apart from other candidates and show your enthusiasm for the industry.
✨Tip Number 4
Prepare for potential scenario-based questions that may arise during interviews. Think about how you would handle specific challenges related to site monitoring and recruitment, as this will showcase your problem-solving skills and practical experience.
We think you need these skills to ace Experienced Clinical Research Associate, Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any independent on-site monitoring you've done. Emphasise your life science degree and any specific protocols or drug indications you've worked with.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for driving healthcare forward. Mention how your skills align with the responsibilities of the CRA role and express your enthusiasm for working with cutting-edge medicines.
Highlight Communication Skills: Since strong communication is key for this role, provide examples in your application of how you've effectively communicated with study sites or team members in previous positions. This could be through presentations, reports, or direct interactions.
Showcase Flexibility and Travel Experience: If you have experience travelling for work or managing multiple sites, make sure to include this in your application. Highlight your ability to adapt to different environments and manage various protocols simultaneously.
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
As a Clinical Research Associate, it's crucial to have a solid understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Brush up on these regulations before your interview, as they are fundamental to the role and will demonstrate your commitment to compliance.
✨Showcase Your Monitoring Experience
Be prepared to discuss your independent on-site monitoring experience in detail. Highlight specific protocols you've handled and how you managed multiple sites. This will show that you have the practical skills needed for the job and can handle the responsibilities effectively.
✨Demonstrate Strong Communication Skills
Effective communication is key in this role. Be ready to provide examples of how you've established lines of communication with study sites and team members. This will illustrate your ability to manage ongoing project expectations and resolve issues efficiently.
✨Express Your Flexibility and Travel Readiness
Since the role requires flexibility and the ability to travel, make sure to convey your willingness to adapt to different situations and locations. Share any past experiences where you successfully managed travel demands while maintaining productivity.
