Centralized Monitoring Lead- Sponsor Dedicated
151.2k - 280.7k PLN151 200 - 280 700 PLN/ rok.UoP
SeniorFull-time·Umowa o pracę
#374875·Dodano dziś·0
Źródło: IQVIATech Stack / Keywords
clinical researchICH GCPclinical trialrisk assessmentdata analyticsMS Officesite monitoringclinical operations
Firma i stanowisko
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Wymagania
- Bachelor's degree in life sciences or related field with minimum 2 years relevant clinical research experience or equivalent.
- Advanced knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws).
- Familiarity with clinical operations systems and software.
- Strong leadership, communication (English), problem-solving, planning, and time management skills.
- Detail-oriented with ability to handle conflicting priorities.
- Proficient in MS Office applications (Word, Excel, PowerPoint).
- Ability to establish effective working relationships and work across cultures.
- Act as a mentor for Central Monitor colleagues.
Obowiązki
Study Start-up:
- Maintain Clinical Operations Plan and support development of study tools/templates.
- Ensure site selection visits are resourced and training compliance is verified.
- Track site activation critical elements and update Clinical Lead and Start-up Lead.
Study Initiations:
- Request monitor resources and verify training compliance for site initiation.
- Coordinate site initiation activities once activation elements are resolved.
Study Maintenance:
- Collaborate with Site Monitor and Clinical Lead on recruitment and compliance.
- Perform ongoing risk assessment through data trending and analytics.
- Manage DTE Alerts and study-specific triggers, follow up on action items.
- Review study documents and site visit reports as applicable.
- Manage resourcing and training for study team members.
- Review and approve Investigator Payments.
- Manage service requests received by CCO staff.
- Provide study updates to Clinical Leads.
Study Closeout:
- Reconcile action items, DTE alerts, and study-specific triggers.
Inne informacje
IQVIA maintains a zero tolerance policy for candidate fraud. False statements or omissions during recruitment will result in disqualification or termination in accordance with applicable law.
IQVIA
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