Skip to main content

Sie sind noch nicht bereit, sich zu bewerben? Melden Sie sich in unserem Talentnetzwerk.

Job Description

Clinical Trials Assistant 1

Sofia, Bulgarien R1457016

Sofia, Bulgarien| Bulgarien

JETZT BEWERBEN

Stellenbeschreibung

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
• High School Diploma or equivalent  Req
• 3 years administrative support experience.
• r.
• 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 English language.
• 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 https://jobs.iqvia.com

JETZT BEWERBEN

Erfahren Sie, Wie Wir Arbeiten

Learn About How We Work

ÄHNLICHE STELLEN

Alle unsere Stellenanzeigen anzeigen MEHR STELLEN ANSEHEN

Registrieren Sie sich in unserem globalen Talentnetzwerk!

Bleiben wir in Kontakt. Melden Sie sich an, um benachrichtigt zu werden, sobald neue Stellenangebote verfügbar sind, welche Ihren Karrierezielen entsprechen.

Registrieren Sie sich in unserem Netzwerk!