İş İlanları Turkey
Site Monitor II
ParexelRemote, TurkeyLaboratory Manager – Pharma Technical Centre (Istanbul)
IMCDTRContract Specialist
Thermo Fisher ScientificTürkiyeRemote SEO Project Manager – My Biz Niche
JobspaddyTurkeySenior Account Manager
Chronos ConsultingTürkiyeSenior Software Engineer (Multiple Stacks) - Remote Contract
Salve.Inno ConsultingTürkiye, TRExperienced Clinical Research Associate
MEDPACETurkeyt-MBA Eğitmeni - Tüm Türkiye
Doğa İKTüm TürkiyeMekanik Teknisyen (Mobil)
DP World AustraliaTürkiyeİmalat Bölümüne Vasıflı Vasıfsız Eleman
istihdamburosu.comTROnline IELTS Course Curator and Methodologist
Etalk Global LtdTROnline Kimya Özel Öğretmeni - Kitu Turkiya
ÖğretmenBulunKitu Turkiya, TurkeyMgr-Human Resources I
Marriott InternationalTürkiyeRegional Operations Manager - Audit, Quality & Compliance
Michael PageTürkiye, TRSafety Engineer
Hyundai Motor Europe GmbHTürkiye, Türkiye, Türkiye, TürkiyeIncome Supervisor
Shangri-LaTürkiyeSenior Digital Designer
InsiderTurkeyAndroid Developer (Hybrid)
Amaris ConsultingTurkeyAccounting and Tax Manager
ElancoTurkey, TRSite Monitor II
ParexelRemote, TurkeyWhen our values align, there's no limit to what we can achieve.
Parexel FSP is currently hiring for a Site Monitor I or II (CRA II / SCRA).
This role is remote from the Istanbul or Ankara regions.
Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is the space where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice we make and every step we take is guided by our unwavering focus on patients, fostering an environment where innovation thrives.
The Site Monitor will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for most activities to supplement on site visit requirements. The Site Monitor will collaborate with the Site Manager to assure that the site follows the protocol and is inspection ready and will coordinate with institutions and investigators at the local level.
Open to Clinical Research Associates with experience of 3 + years of independent onsite monitoring, all types of visits.
A minimum of 3 years’ experience as a clinical monitor (CRA) with demonstrated experience of monitoring onsite.
Experience in managing complex protocols in Oncology or other therapeutic areas (TA’s) where protocols are determined to be high risk.
Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.
Experience of utilizing systems like Siebel Clinical Trial. Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence).
We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work / life balance. We value your welfare just as highly as that of our patients.