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- Tasks: Support clinical trials by managing documentation and ensuring compliance.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on patient outcomes while developing your career.
- Qualifications: Experience in clinical trials and strong communication skills required.
- Other info: Recognised as a top workplace with a commitment to learning and collaboration.
The predicted salary is between 36000 - 60000 £ per year.
We are seeking a Senior Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team. Hybrid working with 3 days per week at sponsor site in Bedfordshire, England.
We share a passion for the work we do, and the impact it has on customers and patients. We are innovative, curious, and feel empowered to explore new ideas and ways of working. We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise. We are committed to growth, always learning, and making the most of agile career opportunities.
Key Responsibilities- Maintain and update clinical systems and documentation, including the Trial Master File.
- Support the preparation, distribution, filing, and archiving of clinical documents and reports.
- Conduct periodic reviews of study files to ensure completeness and compliance.
- Assist with clinical trial supply logistics and tracking.
- Manage Case Report Forms (CRFs), queries, and clinical data flow.
- Serve as a central point of contact for project communications and documentation.
- Previous clinical trials support experience required.
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
- Degree in life sciences or equivalent industry experience.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong written and verbal communication skills in English.
- Excellent time management, organization, and collaboration skills.
Please note: 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!
Senior Clinical Trials Assistant employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Trials Assistant
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their mission and values, especially how they relate to clinical trials. This will help you tailor your answers and show you're genuinely interested.
✨Tip Number 3
Practice common interview questions with a friend or in front of a mirror. Focus on articulating your experience in clinical trials and how it aligns with the role. Confidence is key!
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you're serious about joining our team at IQVIA.
We think you need these skills to ace Senior Clinical Trials Assistant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Trials Assistant role. Highlight your relevant experience in clinical trials and any specific skills that match the job description. We want to see how you can bring your unique flair to our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about clinical trials and how your background aligns with our mission. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Skills: Don’t forget to highlight your proficiency in Microsoft Word, Excel, and PowerPoint. Mention any experience with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. We’re looking for someone 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 innovative team at IQVIA!
How to prepare for a job interview at IQVIA LLC
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your knowledge of clinical trials, especially the regulatory requirements like GCP and ICH. Being able to discuss these topics confidently will show that you're not just familiar with the basics but are genuinely passionate about the field.
✨Showcase Your Organisational Skills
As a Senior Clinical Trials Assistant, you'll need to manage a lot of documentation and logistics. Prepare examples from your past experiences where you've successfully organised complex information or managed multiple tasks simultaneously. This will demonstrate your ability to handle the responsibilities of the role.
✨Communicate Clearly and Effectively
Strong communication skills are key in this role. Practice articulating your thoughts clearly, both verbally and in writing. You might even want to prepare a few questions to ask during the interview to show your engagement and interest in the position.
✨Emphasise Your Teamwork Experience
Collaboration is crucial in clinical trials. Be ready to share specific examples of how you've worked effectively within a team. Highlight any experiences where you brought out the best in others or contributed to a successful project outcome.
