IQVIA

Centralized Monitoring Lead- Sponsor Dedicated

151.2k - 280.7k PLN151 200 - 280 700 PLN/ rok./ rok.UoPUmowa o pracę (brutto)

SeniorOn-site·WarszawaFull-time·Umowa o pracę

#374875·Dodano 4 miesiące temu·1

Źródło: IQVIA

Aplikuj teraz

Tech 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

35 aktywnych ofert

Zobacz wszystkie oferty

Aplikuj teraz