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

Background & Qualifications ??

University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties),
Good level of English,
Minimum 1 years experiences in a CRA and/or study coordinator positions
Strong communication and negotiation skills,
Ability to prioritize and handle multiple tasks,
Effective planning and organizational skills with a result-oriented approach,
Analytical thinking, critical reasoning ability,
Good command of MS Office applications,
No restriction to travel,
Driving License,
No military obligation for male candidates.

Job Description

  • Perform monitoring and site management activities for phase trials projects to assess the progress of clinical projects at assigned investigative/physician sites
  • Ensure clinical project is conducted, recorded, and reported in accordance with the protocol, Company SOPs, ICH-GCP, and all applicable local and legal requirements.
  • May assume clinical functional leadership tasks are assigned, actions as Lead CRA for project
  • Train, support and advise Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
  • Drive performance at the sites. Proactively identify and ensure timely resolution to study-related issues and escalate them as appropriate.
  • Perform regular Site Quality Risk Assessments and adapt monitoring intensity accordingly during the study.
  • Ensure data query resolution in a timely manner.
  • Work with data management to ensure the robust quality of the collected study data.
  • Collaborate with local MSLs as directed by LSM or line manager.

PREFERRED CANDIDATE

POSITION INFORMATION

Firma Sektörü:

İlaç Sanayi

Çalışan Sayısı:

4000-4999