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- Tasks: Join our team to monitor clinical sites and ensure top-notch research practices.
- Company: IQVIA is a global leader in clinical research, driving healthcare innovation.
- Benefits: Enjoy flexible work options, including a potential 4-day work week and an iPad for efficiency.
- Why this job: Be at the forefront of medicine development while growing your career in a supportive environment.
- Qualifications: Life science degree and independent monitoring experience required; 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
- We can offer flexibility regarding site locations to minimize travel. We can also consider candidates looking for a 4 day working week
- As a CRA you will receive an iPad and use of key developments such as site visit app’s, site visit report app’s that allow CRA’s 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
Awards
- FORTUNE Magazine's World's Most Admired Companies list for the fourth year in a row – Ranked #1 in Its Category for the Second Consecutive Year
- Best AI-based Solution for Healthcare” Award in 2023 Artificial Intelligence Breakthrough Awards
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
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
Familiarize 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 at IQVIA, which can be beneficial during your application process.
✨Tip Number 3
Highlight your experience with site monitoring and managing multiple protocols. Be prepared to discuss specific examples of how you've successfully handled challenges in previous roles, as this will showcase your problem-solving skills.
✨Tip Number 4
Research IQVIA's recent projects and innovations in clinical research. Being knowledgeable about their work will allow you to ask informed questions during interviews and show your genuine interest in contributing to their mission.
We think you need these skills to ace Experienced Clinical Research Associate, Sponsor Dedicated
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Experienced Clinical Research Associate position. Understand the responsibilities and requirements, especially the importance of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Highlight Relevant Experience: In your application, emphasize your independent on-site monitoring experience and any relevant life science degree. Mention specific protocols and sites you have handled, showcasing your ability to manage multiple projects effectively.
Showcase Communication Skills: Since strong communication skills are essential for this role, provide examples in your application that demonstrate your written and presentation abilities. This could include experiences where you successfully communicated with study teams or managed site expectations.
Tailor Your CV and Cover Letter: Customize your CV and cover letter to align with the job description. Use keywords from the posting, such as 'site monitoring visits', 'subject recruitment plan', and 'regulatory submissions', to ensure your application stands out.
How to prepare for a job interview at IQVIA
✨Understand the Role and Responsibilities
Make sure you thoroughly understand the responsibilities of a Clinical Research Associate. Familiarize yourself with site monitoring visits, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This knowledge will help you answer questions confidently and demonstrate your suitability for the role.
✨Showcase Your Experience
Prepare to discuss your previous experience in independent on-site monitoring and handling multiple protocols. Be ready to provide specific examples of how you've successfully managed studies and addressed challenges. This will highlight your capability and readiness for the position.
✨Highlight Your Communication Skills
As a CRA, strong communication skills are essential. Be prepared to discuss how you establish lines of communication with sites and manage ongoing project expectations. Share examples of how you've effectively communicated complex information to diverse stakeholders.
✨Demonstrate Flexibility and Adaptability
The job requires flexibility regarding site locations and travel. Be ready to discuss your willingness to adapt to changing circumstances and how you've successfully navigated similar situations in the past. This will show that you're a good fit for the dynamic nature of the role.
