DevOps Engineer at Workiz
Workiz51 – 200 Xodimlar
SaaS
Improve Kubernetes, cloud infrastructure, CI/CD, observability, and cost efficiency for Workiz’s home-services software platform.
Ochish
TFS HealthScience - Contract Research Organization klinik rivojlanishning barcha bosqichlarida biotexnologiya va farmatsevtika kompaniyalarini qo‘llab-quvvatlovchi global shartnoma asosidagi tadqiqot tashkilotidir. Uning xizmatlari I–III bosqichdagi klinik sinovlar, IV bosqichdagi real hayot ma’lumotlari tadqiqotlari va strategik resurs bilan ta’minlashni qamrab oladi. Kompaniya dermatologiya, ichki kasalliklar, neyrofan, onkologiya va gematologiya, oftalmologiya, pediatriya, kam uchraydigan kasalliklar hamda yetim dorilar yo‘nalishlarida tajribaga ega. Kompaniya to‘liq xizmat ko‘rsatuvchi CROning imkoniyatlari va xalqaro qamrovini o‘rta hajmdagi tashkilotga xos moslashuvchanlik hamda shaxsiylashtirilgan hamkorlik bilan birlashtiradi.
Senior Clinical Research Associate, Oncology (Contract, Italy Remote)
Home-based Senior Clinical Research Associate role supporting oncology trials for TFS HealthScience. Responsibilities include site monitoring, compliance oversight, documentation, reporting, and trial-system updates.
Italiya42 000 € – 58 000 € / yil
MasofaviyShartnomaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqotTavsif
- Serve as an operational member of the project team
- Open, monitor both on-site and remotely, and close clinical trial sites
- Conduct trial monitoring in line with company and sponsor SOPs, GCP, ICH guidelines, and applicable regulations
- Carry out monitoring activities that protect subject safety and support data integrity and study quality
- Confirm proper informed consent processes and adherence to study protocols
- Assess electronic and paper CRFs and source records for accuracy and validity
- Check investigational product management and accountability
- Prepare Monitoring Visit Reports, record findings and corrective or preventive actions, maintain tracking systems, and escalate concerns
- Communicate identified issues and required follow-up actions to study sites
- Submit site documentation to the eTMF or paper TMF and confirm Investigator Site File upkeep
- Support preparation for audits and inspections and complete related follow-up
- Order, ship, and reconcile clinical investigation supplies when required
- Maintain accurate site information in CTMS and other project systems
Talablar
- Bachelor’s degree in life sciences or nursing preferred, or an equivalent qualification
- At least three years of clinical trial monitoring experience in oncology, including at least one Phase I or Phase II study
- Working knowledge of medical terminology and the science relevant to assigned drugs and therapeutic areas
- Knowledge of Good Clinical Practice regulations and ICH guidelines
- Capacity to work independently within a matrixed team environment
- Strong written and spoken communication skills
- Fluency in English
- Highly organized approach to work
- Confidence with technology, software, and computer applications
- Willingness and ability to travel up to 60–80%, including overnight and international travel where applicable
Imtiyozlar
- Competitive compensation package
- Comprehensive benefits offering
- Opportunities for personal and professional development
- Lunch vouchers
- Health insurance
- Pension plan
- Car allowance where applicable
- Collaborative, innovative working environment
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