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Clinical Research Administrative

ALVIMEDICA

İstanbul(Avr.)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Position Level

Specialist

Department

Health / Medical

Health / Medical

Application Count

495 application

Job Type

Full-Time

Position Level

Specialist

Application Count

495 application

Department

Health / Medical

QUALIFICATIONS AND JOB DESCRIPTION

We are looking for a Clinical Research Administrative having the following qualifications to be employed in our factory located in ÇATALCA.

  • 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


İŞ TANIMI

  • 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

More than 2 years of experience
Bachelor’s(Graduate), Master’s(Student), Master’s(Graduate), Doctorate(Student), Doctorate(Graduate)
Completed, Exempt

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

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

Health / Medical products

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

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