Clinical Trial Assistant

Clinical Trial Assistant

Full-Time 28800 - 43200 £ / year (est.) No working from home possible
IQVIA LLC

At a Glance

  • Tasks: Support clinical trials by managing documentation and assisting research teams.
  • Company: Join IQVIA, a leader in global clinical research and healthcare intelligence.
  • Benefits: Gain world-class training, competitive salary, and opportunities for professional growth.
  • Other info: Diverse and inclusive workplace with excellent career advancement potential.
  • Why this job: Make a real impact in healthcare while working with innovative technology.
  • Qualifications: Strong communication skills and basic knowledge of clinical research regulations.

The predicted salary is between 28800 - 43200 £ per year.

Clinical Trial Assistant page is loaded## Clinical Trial Assistantlocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: October 31, 2025 (21 days left to apply)job requisition id: R1508510IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.As a Clinical Trial Assistant within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CTAs.With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.**Essential Functions of a Clinical Trial Assistant (CTA)*** Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.* Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.* Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.* Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.* Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.* May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.* May perform assigned administrative tasks to support team members with clinical trial execution.**Required Knowledge and Skills*** Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines* Knowledge of applicable protocol requirements as provided in company training* Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint* Good written and verbal communication skills including excellent command of English* Effective time management and organizational skills* Ability to establish and maintain effective working relationships with coworkers, managers and clients\\*Please note - this role is not eligible for UK visa sponsorship\\**IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.*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 atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr

Clinical Trial Assistant employer: IQVIA LLC

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Reading, Berkshire. As a Clinical Trial Assistant, you will benefit from world-class training and professional development opportunities, empowering you to grow your career while contributing to meaningful advancements in healthcare. Our commitment to diversity and inclusion ensures a supportive environment where every employee can thrive and make a real impact on patient outcomes globally.

IQVIA LLC

Contact Details:

IQVIA LLC Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Trial Assistant

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like IQVIA LLC. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like IQVIA LLC.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like IQVIA LLC. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what IQVIA LLC is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Clinical Trial Assistant

Knowledge of Good Clinical Practice (GCP)
Understanding of International Conference on Harmonization (ICH) guidelines
Clinical documentation management
Case Report Form (CRF) tracking
Microsoft Word proficiency
Microsoft Excel proficiency
Microsoft PowerPoint proficiency

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at IQVIA LLC!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show IQVIA LLC that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at IQVIA LLC!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At IQVIA LLC, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at IQVIA LLC

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IQVIA LLC that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with IQVIA LLC’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.