Clinical Research Specialist Alvimedica

İstanbul(Avr.)(Çatalca)

Nasıl hesaplanır?
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Son iş deneyimin, geçmiş deneyimlerin ve toplam deneyimin uygunluk puanını etkileyen kriterler arasındadır.
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Mesleki Yeterlilikler
Şirketlerin ilanda belirlediği kriterlerle özgeçmişindeki bilgilerin ne kadar uyumlu olduğu içerik karşılaştırılmasıyla bulunur.
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Diğer Bilgiler

QUALIFICATIONS AND JOB DESCRIPTION


QUALIFICATIONS 

We are looking for a Clinical Research Specialist 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
  • 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

POSITION INFORMATION