Arama önerileri:

part time
şoför
günlük
home office
garson
asistan
yönetici asistanı
danışma görevlisi
vasıfsız eleman
öğretmen
psikolog
anaokulu öğretmeni
bayan eleman
Ankara
İzmir
Istanbul
Ankara
Antalya
Gebze
Bursa

Clinical Trials Assistant (Single Sponsor) Turkey

IQVIA
Istanbul
Tam zamanlı
3 gün önce

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 Degree or equivalent

  • 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 co-workers, 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

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