Internal Job Description
IQVIA are seeking a Clinical Trial Assistant to join us on our mission to drive healthcare forward. Hybrid working available from either Luton or High Wycombe offices (2–3 days per week), depending on your location and business needs. A fully remote contract may be considered for specific projects.
Sr. Clinical Trial Assistant will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

QUALIFICATIONS / EXPERIENCE

• Minimum 8-16 months of clinical trial assistance experience
• Life science degree educated or equivalent industry experience.
• Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines preferred.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.co

ESSENTIAL FUNCTIONS

• Assist Clinical Research Associates and Regulatory and Start-Up team with updating and maintaining clinical documents and systems (e.g., Trial Master File)
• Assist the clinical team with 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 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.