At a Glance
- Tasks: Support clinical teams in managing trial documents and supplies for impactful healthcare research.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain hands-on experience in a dynamic environment with growth opportunities.
- Other info: Collaborative culture with a focus on professional development.
- Why this job: Make a difference in healthcare by contributing to innovative medical treatments.
- Qualifications: Life science degree or equivalent experience; knowledge of GCP and ICH guidelines preferred.
The predicted salary is between 30000 - 42000 € per year.
Overview
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
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the healthcare sector. Our Clinical Trial Assistants benefit from comprehensive training and development opportunities, ensuring personal and professional growth while contributing to meaningful projects that drive healthcare forward. Located in a vibrant area, our team enjoys a supportive environment that values work-life balance and encourages open communication.
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 trial field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Trial Assistant role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and ICH guidelines. We recommend having specific examples ready to showcase your experience and skills related to clinical documentation and data management.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for openings at IQVIA, where you can find roles that truly resonate with your aspirations.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which are key traits for a Clinical Trial Assistant.
We think you need these skills to ace Clinical Trial Assistant in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Trial Assistant role. Highlight any relevant experience you have in clinical trials, and don’t forget to mention your knowledge of GCP and ICH guidelines. We want to see how your background fits with 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 research and how your skills can help us drive healthcare forward. Keep it concise but engaging – we love a good story!
Show Off Your Communication Skills:Since this role involves a lot of communication, make sure your written application reflects your strong command of English. Use clear and professional language, and double-check for any typos or grammatical errors. We appreciate attention to detail!
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, you’ll find all the info you need about the role and our company there!
How to prepare for a job interview at IQVIA
✨Know Your Clinical Basics
Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these concepts confidently will show that you understand the framework within which you'll be working.
✨Showcase Your Organisational Skills
Since this role involves a lot of document handling and tracking, prepare examples from your past experience where you successfully managed multiple tasks or projects. Highlight your time management strategies and how you ensured everything was completed accurately and on time.
✨Communicate Effectively
Practice your verbal and written communication skills before the interview. You might be asked to explain complex information clearly, so think about how you can convey your ideas simply and effectively. Consider doing a mock interview with a friend to refine your delivery.
✨Be Ready for Teamwork Questions
This position requires collaboration with various teams, so expect questions about teamwork. Prepare specific examples of how you've worked well with others in the past, focusing on your ability to build relationships and communicate effectively with colleagues and clients.
