Hybrid Senior Clinical Trials Support Specialist in Reading
Hybrid Senior Clinical Trials Support Specialist

Hybrid Senior Clinical Trials Support Specialist in Reading

Reading Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support clinical trials by managing documentation and logistics while ensuring compliance.
  • Company: Leading global clinical research provider with a focus on impactful work.
  • Benefits: Hybrid working model, continuous learning, and development opportunities.
  • Why this job: Make a real difference in clinical research while growing your career.
  • Qualifications: Experience in clinical trials, life sciences degree, and Microsoft Office skills.
  • Other info: Join a dynamic team dedicated to advancing healthcare.

The predicted salary is between 36000 - 60000 £ per year.

A leading global clinical research provider is seeking a Senior Clinical Trials Assistant in Reading, UK. This role involves maintaining clinical documentation, supporting trial logistics, and ensuring compliance with regulations.

The ideal candidate will have previous experience in clinical trials, a degree in life sciences, and proficiency in Microsoft Office.

Join us for a career that makes an impact and offers continuous learning and development opportunities. Hybrid working model with 3 days on-site in Bedfordshire.

Hybrid Senior Clinical Trials Support Specialist in Reading employer: IQVIA

As a leading global clinical research provider, we pride ourselves on fostering a dynamic work culture that prioritises employee growth and development. Our hybrid working model allows for flexibility while ensuring you are part of a collaborative team in Reading, UK, where you can make a meaningful impact in the field of clinical trials. With continuous learning opportunities and a commitment to compliance and excellence, we offer an environment where your contributions are valued and recognised.
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Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Hybrid Senior Clinical Trials Support Specialist in Reading

✨Tip Number 1

Network like a pro! Reach out to professionals in the clinical trials field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors for you.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of clinical trial regulations and logistics. We recommend practising common interview questions with a friend to boost your confidence.

✨Tip Number 3

Showcase your skills! Bring along examples of your previous work in clinical trials to discuss during interviews. We love seeing how you’ve made an impact in past roles.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see what you bring to the table!

We think you need these skills to ace Hybrid Senior Clinical Trials Support Specialist in Reading

Clinical Documentation Management
Trial Logistics Support
Regulatory Compliance
Experience in Clinical Trials
Degree in Life Sciences
Proficiency in Microsoft Office
Attention to Detail
Communication Skills
Problem-Solving Skills
Organisational Skills
Team Collaboration
Adaptability
Continuous Learning

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical trials and any relevant qualifications. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

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 impactful – we love a good story!

Showcase Your Tech Skills: Since proficiency in Microsoft Office is key, make sure to mention any specific tools or software you’re comfortable with. We appreciate candidates who can hit the ground running with tech!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at IQVIA

✨Know Your Clinical Trials Inside Out

Make sure you brush up on your knowledge of clinical trials and the specific regulations that govern them. Familiarise yourself with common challenges faced in trial logistics and how to overcome them, as this will show your potential employer that you're not just knowledgeable but also proactive.

✨Showcase Your Life Sciences Background

Since a degree in life sciences is essential for this role, be prepared to discuss how your educational background has equipped you for the position. Highlight any relevant projects or experiences that demonstrate your understanding of clinical research and its impact on patient care.

✨Demonstrate Your Microsoft Office Skills

Proficiency in Microsoft Office is a must-have, so be ready to provide examples of how you've used these tools in previous roles. Whether it's creating reports, managing data, or coordinating schedules, showcasing your skills will give you an edge over other candidates.

✨Embrace the Hybrid Working Model

With a hybrid working model in place, express your adaptability and willingness to work both on-site and remotely. Share any past experiences where you've successfully managed your time and tasks in a flexible work environment, as this will reassure the interviewer of your ability to thrive in their setup.

Hybrid Senior Clinical Trials Support Specialist in Reading
IQVIA
Location: Reading

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  • Hybrid Senior Clinical Trials Support Specialist in Reading

    Reading
    Full-Time
    36000 - 60000 £ / year (est.)
  • I

    IQVIA

    10000+
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