Clinical Trial Assistant

2 weeks ago


Remote, United Kingdom IQVIA Full time
Do you want to grow your career with the World's largest CRO?

We offer genuine career progression (named on LinkedIn's "

Top Companies:
The 25 best workplaces to grow your career in the UK"), supportive leadership, team spirit, a broad learning experience and impactful work.

Job Overview

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.


Responsibilities

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  • Collaborate with clinical team on 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 and completeness.
  • Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Coordinate 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.
  • Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
  • Assist with training and onboarding of new CTAs.
  • May lead CTA study teams.
  • May assist with interviewing and screening of potential new team members
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
  • May participate in departmental quality or process improvement initiatives.

We are looking for:

  • Experience of providing administrative support to Clinical Trials. Ideally experience of supporting Clinical Research Associates OR Regulatory and Start-Up teams
  • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Effective time management and organizational skills.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Effective written and verbal communication skills including good command of English language.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**#LI-Remote #LI-AdamThompson

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