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İstanbul(Avr.)(Avcılar, Bakırköy, Bayrampaşa, Bağcılar, Bahçelievler, Beşiktaş, Beyoğlu, Büyükçekmece, Çatalca, Esenler, Eyüp, Eminönü, Fatih, Gaziosmanpaşa, Güngören, Kağıthane, Küçükçekmece, Sarıyer, Silivri, Şişli, Zeytinburnu, Beylikdüzü, Mimarsinan/Büyükçekmece, Sultangazi, Arnavutköy, Başakşehir, Esenyurt), İstanbul(Asya)(Adalar, Beykoz, Kadıköy, Kartal, Maltepe, Pendik, Sultanbeyli, Şile, Tuzla, Ümraniye, Üsküdar, Çekmeköy, Ataşehir, Sancaktepe)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Position Level

Specialist

Department

Application Count

209 application

Job Type

Full-Time

Position Level

Specialist

Application Count

209 application

Department

QUALIFICATIONS AND JOB DESCRIPTION

  • University degree in life sciences (Pharmacy, Biology, Chemistry, Genetics, Medicine or a related field),
  • Minimum 3 years of on-site monitoring experience in clinical studies,
  • Excellent command of written and spoken English,
  • Good knowledge of MS Office applications,
  • Strong project management skills together with a solution oriented teamwork attitude,
  • Self-motivated personality,
  • Good communication skills at all levels,
  • Good time management, presentation, planning and organizational skills,
  • Exceptional attention to detail,
  • Ability to travel (Valid passport required in the case of international business travel)
  • No military obligation. (for male candidates) 


İŞ TANIMI

We are looking for a Junior Project Manager to become a team member for local and international clinical studies.

Brief Job Description:

The candidate will be responsible for conducting clinical studies, managing & monitoring study sites in accordance with Study Protocols, SOPs, ICH-GCP (International Clinical Harmonization-Good Clinical Practice) and local regulations. She/he will manage multiple projects, support Project Teams and report directly to a Senior Project Manager locally and abroad.

She/he will also be responsible for coordinating all necessary activities required to set up a study, participating in the start-up processes including reviewing protocols, reviewing Case Report Forms (CRFs), preparing Informed Consent Forms (ICFs), developing study documents, organizing investigator and study specific training meetings, presenting study related material and ensuring that the study meets  planned timelines and  high quality data is generated.

Preferred Candidate

3 - 5 years of experience
Bachelor’s(Graduate), Master’s(Graduate), Doctorate(Graduate)
Completed

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

Proje Müdürü Proje Müdürü Maaşları Proje Müdürü Nasıl Olunur? Proje Müdürü Nedir? Proje Müdürü İş İlanları
Hakkımızda

MONITOR CRO Monitor CRO was founded in İstanbul (1999), as a pioneering Contract Research Organization in Turkey. We are currently the lead

Şirket Sayfasına Git
Şirketin Aydınlatma Metni

6698 sayılı Kişisel Verilerin Korunması Hakkında Kanun (“KVKK”) uyarınca, Monitor Medikal Araştırma

Detaylı Bilgi

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

Proje Müdürü Proje Müdürü Maaşları Proje Müdürü Nasıl Olunur? Proje Müdürü Nedir? Proje Müdürü İş İlanları