Clinical Trial Assistant in Reading
Clinical Trial Assistant

Clinical Trial Assistant in Reading

Reading Full-Time 28800 - 43200 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support clinical trials by managing documentation and assisting with site compliance.
  • Company: Join IQVIA, a leader in global clinical research and healthcare intelligence.
  • Benefits: Gain world-class training, competitive salary, and opportunities for professional growth.
  • Why this job: Make a real impact in healthcare while working with cutting-edge technology.
  • Qualifications: Strong communication skills and basic knowledge of clinical research regulations.
  • Other info: Dynamic work environment with a focus on diversity and inclusion.

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

IQVIA 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.

Clinical Trial Assistant in Reading employer: IQVIA LLC

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. As a Clinical Trial Assistant in Reading, you'll benefit from world-class training and professional development opportunities, enabling 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.
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Contact Detail:

IQVIA LLC Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trial Assistant in Reading

✨Tip Number 1

Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at local events. A friendly chat can lead to opportunities that aren’t even advertised yet.

✨Tip Number 2

Prepare for interviews by researching IQVIA and their projects. Show us you’re passionate about clinical trials and have a solid understanding of the role. We love candidates who come prepared!

✨Tip Number 3

Practice your communication skills! As a Clinical Trial Assistant, you’ll need to convey information clearly. Try mock interviews with friends or use online resources to polish your verbal skills.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re serious about joining our team at IQVIA.

We think you need these skills to ace Clinical Trial Assistant in Reading

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
Written communication skills
Verbal communication skills
Time management skills
Organisational skills
Ability to establish effective working relationships
Attention to detail
Adaptability

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Assistant role. Highlight any relevant experience, especially in clinical research or related fields. We want to see how your skills match what we're looking for!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how you can contribute to our team. Keep it concise but engaging – we love a good story!

Show Off Your Skills: Don’t forget to showcase your computer skills and communication abilities. Mention your familiarity with tools like Microsoft Word and Excel, as well as your understanding of GCP and ICH guidelines. We’re keen on candidates who can hit the ground running!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at IQVIA!

How to prepare for a job interview at IQVIA LLC

✨Know Your Regulations

Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these regulations confidently will show that you understand the framework within which clinical trials operate.

✨Showcase Your Organisational Skills

As a Clinical Trial Assistant, you'll need to juggle multiple tasks. Prepare examples of how you've effectively managed your time and organised projects in the past. This will demonstrate your ability to handle the demands of the role.

✨Brush Up on Your Tech Skills

Make sure you're comfortable with Microsoft Word, Excel, and PowerPoint. You might be asked about your experience with these tools, so be ready to share specific instances where you've used them to support your work.

✨Communicate Clearly

Good written and verbal communication skills are essential. Practice articulating your thoughts clearly and concisely. You could even prepare a few questions to ask during the interview to show your engagement and interest in the role.

Clinical Trial Assistant in Reading
IQVIA LLC
Location: Reading
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  • Clinical Trial Assistant in Reading

    Reading
    Full-Time
    28800 - 43200 £ / year (est.)
  • I

    IQVIA LLC

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