Clinical Trial Assistant 2 Sponsor Dedicated- Prague
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Job Location:
Prague - Czech Republic
Monthly Salary:
Not Disclosed
Posted on:
18 hours ago
Vacancies:
1 Vacancy
Job Summary
We are leaders in innovation and first to new technologies meaning a vast amount of career development opportunities are available.
As Clinical Trial Assistant you will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials.
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.
Essential Functions
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.
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.
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Qualifications
Bachelors Degreein Science
Administrative support experience is a plus.
Equivalent combination of education training and experience.
Computer skills including working knowledge of Microsoft Word Excel and PowerPoint.
Written and verbal communication skills including good command of Czech and English languages.
Effective time management and organizational skills.
Ability to establish and maintain effective working relationships with coworkers managers and clients.
Awareness of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Knowledge of applicable protocol requirements as provided in company training.
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
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
