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


Ascot Science  is a full-service clinical contract research organization (CRO) founded in 2016 in Istanbul. We provide Phase I-IV clinical development services to the pharmaceutical industry.

The Clinical Research Associate position at Ascot Science offers the unique opportunity to have an exciting career in the clinical research area.

Responsibilities 

  • To verify that the conduct of the study is in compliance with the currently approved protocol/amendment(s), with GCP, and with the applicable regulatory requirement(s), and report any deviation as per study procedure
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
  • When requested to support preparation of regulatory and / or EC submission
  • Investigational product/drug accountability and inventory;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  • Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications :

  • Must have a minimum of a bachelor’s degree in a health or science related field
  • Minimum 2 years healthcare-related work experience preferred
  • Advanced English 
  • No limitation for travel
  • Strong communication and presentation skills
  • Familiar to work in accordance with the sponsor and company SOPs
  • Ability to manage the time, prioritizationfollow up processes adequately


PREFERRED CANDIDATE

POSITION INFORMATION

Firma Sektörü:

Sağlık, İlaç Sanayi

Çalışan Sayısı:

1-24