Clinical Trial Assistant

Nanosep AB; Reading; Hybrid; GBP 25,000 - 35,000; Full time

Job summary

A leading global provider of clinical research is seeking a Clinical Trial Assistant to support daily administrative tasks and ensure compliance in clinical trials. This role involves collaboration with various teams and offers remote work with some on-site requirements. Ideal candidates will have a degree in life sciences and some clinical trial experience, along with strong communication and organizational skills.

Qualifications

• Ideally 6-12 months of clinical trial experience.
• Knowledge of GCP and ICH guidelines.

Responsibilities

• Assist CRAs with updating and maintaining clinical documents.
• Conduct periodic reviews of study files for completeness.
• Serve as a central contact for project communications.

Skills

Communication

Time Management

Organizational Skills

Education

Degree in life sciences

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

IQVIA cFSP (sponsor-dedicated) is seeking a Clinical Trial Assistant to join us in our mission to advance healthcare.

The Clinical Trial Assistant will perform daily administrative tasks in collaboration with Clinical Research Associates and Regulatory and Start-Up teams to ensure accurate and complete Trial Master File delivery.

This role offers remote work with occasional on-site requirements in Buckinghamshire.

Essential Functions

• Assist CRAs and RSU team with updating and maintaining clinical documents and systems, such as the Trial Master File (TMF), ensuring site compliance and timely project delivery.
• Collaborate on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports following SOPs.
• Conduct periodic reviews of study files for completeness.
• Support the preparation, handling, and distribution of Clinical Trial Supplies and maintain tracking information.
• Manage tracking of Case Report Forms (CRFs), queries, and clinical data flow.
• Serve as a central contact for project communications and documentation within the clinical team.

Qualifications

• Degree in life sciences or equivalent industry experience.
• Ideally 6-12 months of clinical trial experience and knowledge of GCP and ICH guidelines.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong written and verbal communication skills in English.
• Good time management and organizational skills.
• Ability to build effective working relationships with colleagues, managers, and clients.

Please note: this role is not eligible for UK visa sponsorship.

IQVIA is a leading global provider of clinical research, commercial insights, and healthcare intelligence, dedicated to accelerating medical development and improving patient outcomes worldwide. Learn more at https://jobs.iqvia.com.

We value diverse talent with innovative minds committed to impact. Everyone at IQVIA contributes to our goal of helping customers improve lives globally. Thank you for your interest in growing your career with us.

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