Clinical Trials Assistant Jobs at IQVIA, UK | Life Sciences Candidates, Apply Now
A rare chance has emerged for aspiring professionals as IQVIA seeks a Clinical Trials Assistant in Reading, United Kingdom. This full-time hybrid role offers an exciting opportunity to contribute to clinical trials and support innovative healthcare solutions, making it a highly sought-after position in the field of clinical trials assistant jobs in the UK.
- Job Position: Clinical Trials Assistant
- Location: Reading, United Kingdom
- Reference Number: R1563431
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization is dedicated to accelerating innovation for a healthier world by creating intelligent connections that enhance the development and commercialization of medical treatments. With a commitment to integrity and excellence, IQVIA is recognized as one of the best places to work in the UK, making it a prime choice for those seeking clinical trials assistant jobs.
Clinical Trial Assistant Role: Job Description
The Clinical Trials Assistant will join the cFSP (sponsor-dedicated) team and will be required to commit to ad-hoc travel to the sponsor’s office in Maidenhead, Berkshire. This role involves maintaining clinical systems and documentation, supporting the preparation and filing of clinical documents, and ensuring compliance with regulatory requirements. This position is ideal for those looking to advance their careers in clinical trials assistant vacancies.
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.
Eligibility Criteria
For clinical trials assistant jobs, candidates should meet the following requirements:
- 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.
Why Join IQVIA?
- IQVIA shares a passion for the work it does, and the impact it has on customers and patients.
- The organization fosters an innovative and curious environment, empowering employees to explore new ideas.
- Collaboration is key, bringing out the best in each other and maximizing diverse skills and perspectives.
- IQVIA is committed to growth, offering agile career opportunities and continuous learning.
- Recognized as a top employer, IQVIA has been listed as one of the best places to work in the UK.
IQVIA is offering clinical trials assistant jobs that provide a unique opportunity to contribute to significant healthcare advancements. Qualified candidates are encouraged to apply for this clinical trials assistant vacancy and take the next step in their career in clinical trials jobs in the UK. Applications should be submitted at the earliest to ensure consideration.
