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İstanbul(Avr.)(Çatalca)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Position Level

Specialist

Department

Health / Medical

Health / Medical

Application Count

477 application

Job Type

Full-Time

Position Level

Specialist

Application Count

477 application

Department

Health / Medical

QUALIFICATIONS AND JOB DESCRIPTION

QUALIFICATIONS 

We are looking for a Clinical Research Specialist having the following qualifications to be employed in our factory 

  • Appropriate education level: Min. BSc. or Masters degree (from Biology, Molecular Biology, Bioengineering or related science departments)
  • At least 2 year experience in Clinical Reseach, preferable in a position as Clinical Research Administrative,
  • Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice and ICH guidelines,
  • Advanced in English both spoken and written,
  • Experience in global clinical studies is a plus,
  • No military obligations for male candidates,
  • Excellent communication and presentation skills,
  • No restrictions to travel frequently
  • Must have medical device experience.

JOB DESCRIPTION

  • Develop and write Clinical study protocols, Case Report Forms, Informed Consent, Investigator’s Brochure, Interim and Final Study Reports, Safety Reporting Reports, Site Visit Reports and any other relevant documents in accordance to the ICH-GCP, ISO14155 and applicable global regulations.
  • Coordinate the communication with the Ethics Committee and Competent Authorities; perform regulatory authority applications and approvals of clinical studies, study reporting and safety reporting to these authorities according to the applicable standards and regulations.
  • Monitor the clinical trials throughout its duration, which involves visiting the trial sites on a regular basis; perform Site Initiaition Visit (SIV), Monitoring Visits (MV) and Close Out Visit (COV) and prepare the Reports.
  • Communicate with the investigator and study staff to ensure the proper ongoing of the clinical study.
  • During the site visits, verify that data entered on to the CRFs as the source data/document verification (SDV) and collect completed CRFs.

Preferred Candidate

5 - 10 years of experience
Bachelor’s(Graduate), Master’s(Graduate)
Completed

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

Klinik Araştırma Uzmanı Klinik Araştırma Uzmanı Maaşları Klinik Araştırma Uzmanı Nasıl Olunur? Klinik Araştırma Uzmanı Nedir? Klinik Araştırma Uzmanı İş İlanları
Hakkımızda

ALVIMEDICA1997 yılında, tek kullanımlık tıbbi ürünler; tedavi amaçlı damar içi protezler tasarlamak ve üretmek amacıyla, Nemed Limited Şirketi olarak

Şirket Sayfasına Git

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

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