warning
İlan yayından kaldırılmıştır

Clinical Trial Assistant (Cta)

IQVIA

İstanbul(Avr.)(Şişli)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Years of Experience

No experience preference

Department

Health / Medical

Health / Medical

Application Count

232 application

Job Type

Full-Time

Years of Experience

No experience preference

Application Count

232 application

Department

Health / Medical

QUALIFICATIONS AND JOB DESCRIPTION

Clinical Trials Assistant

 

IQVIA  is the world’s leading information, services and technology company dedicated to making healthcare perform better.


Drawing on information from 100,000 suppliers, and on insights from more than 55+ billion healthcare transactions processed annually, IQVIA’s approximately 10,000 professionals drive results for over 5,000 healthcare clients globally.

 IQVIA is looking for a CTA in Clinical Operations department;·       


Main Responsibilities

o   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.

o   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.

o   Assist with periodic review of study files for completeness.

o   Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

o   Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Qualifications

o   High School Diploma or equivalent  

o   3 years administrative support experience.

o   Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.

o   Written and verbal communication skills

o   Arabic and English language are required.

o   Effective time management and organizational skills.

o   Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

o   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.

o   Knowledge of applicable protocol requirements as provided in company training.


Preferred Candidate

Bachelor’s(Graduate)
Turkish(Reading : Advanced, Writing : Advanced, Speaking : Advanced) English(Reading : Advanced, Writing : Advanced, Speaking : Advanced) Arabic(Reading : Advanced, Writing : Advanced, Speaking : Advanced)

Klinik Araştırma Asistanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Klinik Araştırma Asistanı Klinik Araştırma Asistanı Maaşları Klinik Araştırma Asistanı Nasıl Olunur? Klinik Araştırma Asistanı Nedir? Klinik Araştırma Asistanı İş İlanları

Pharmaceuticals industry / Health services

Hakkımızda

Biz IQVIA’yız, Beşeri Veri Bilimi Şirketi Dünya çapında 100’den fazla ülkede, 50.000’den fazla kişiden oluşan dev bir ekiple, sağlık sektöründe faaliy

Şirket Sayfasına Git
Yan Haklar

Özel Sağlık Sigortası, Servis, Yemek Kartı (Setcard, Ticket, Multinet, Sodexo vb.), Yemekhane, Hayat Sigortası.

Klinik Araştırma Asistanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Klinik Araştırma Asistanı Klinik Araştırma Asistanı Maaşları Klinik Araştırma Asistanı Nasıl Olunur? Klinik Araştırma Asistanı Nedir? Klinik Araştırma Asistanı İş İlanları