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- Tasks: Join a structured training programme to conduct clinical monitoring visits and ensure study compliance.
- Company: IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Gain hands-on experience, competitive salary, and opportunities for continuous learning.
- Why this job: Make a real impact in healthcare while developing your skills in a supportive environment.
- Qualifications: Bachelor's or Master's in a scientific discipline; knowledge of clinical research regulations preferred.
- Other info: Collaborative culture with excellent career growth opportunities in the life sciences sector.
The predicted salary is between 36000 - 60000 £ per year.
Engage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Essential Functions
- Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
- Gain experience in study procedures by working with experienced clinical staff.
- Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
- Under close supervision, administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Under close supervision, 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.
- Under close supervision, 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 Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
- Under close supervision may support start-up phase.
- Under close supervision, 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, learn key facets for successful development of project subject recruitment plan on a per site basis.
- Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability.
- Assist in tracking subject site recruitment progress.
Qualifications
- Bachelor's or Master's Degree in scientific discipline or health care preferred.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Experience within CRO, hospital or nursing setting preferred.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Right to work in the United Kingdom required, 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.
Associate CRA employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate CRA
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be when it comes to landing that Associate CRA role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and ICH guidelines. We recommend practising common interview questions with a friend or even in front of the mirror. Confidence is key, and knowing your stuff will help you shine!
✨Tip Number 3
Showcase your enthusiasm for learning! During interviews, let them know you’re eager to engage in their structured training programme. We believe that a positive attitude towards growth can set you apart from other candidates.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Associate CRA
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Associate CRA role. Highlight any relevant experience in clinical research, and don’t forget to mention your knowledge of GCP and ICH guidelines. We want to see how your background fits with what we do!
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 team. Keep it concise but engaging – we love a good story!
Showcase Your Skills: Don’t just list your skills; show us how you’ve used them in real situations. Whether it’s your computer skills or your ability to communicate effectively, give us examples that demonstrate your capabilities.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at IQVIA
✨Know Your Stuff
Make sure you brush up on clinical research regulations like GCP and ICH guidelines. Familiarise yourself with the job description and be ready to discuss how your background aligns with the responsibilities of an Associate CRA.
✨Showcase Your Communication Skills
Since this role involves liaising with study teams and site staff, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated in past roles, especially in challenging situations.
✨Demonstrate Your Team Spirit
This position requires collaboration with various stakeholders. Think of instances where you've worked well in a team, and be ready to share how you contributed to achieving common goals.
✨Ask Smart Questions
Prepare insightful questions about the company's projects, culture, and expectations for the role. This shows your genuine interest and helps you determine if it's the right fit for you.