Local Trial Manager - Sponsor Dedicated

Local Trial Manager - Sponsor Dedicated

Vollzeit Kein Homeoffice möglich
I

Overview

In this role you oversee local trial delivery for a single client within IQVIA’s Clinical FSP team, ensuring trials run on time, within budget, and in compliance. You’ll coordinate cross-functional country activities, manage vendor and contract aspects, and support quality programs and inspections. The position emphasizes patient safety, regulatory compliance, and data integrity across Austria, with a focus on oncology studies. You will shape local recruitment, budget execution, and country-level trial governance, in a hybrid home-based setup.

Leistungen / Benefits

  • home-based throughout Austria
  • market-competitive gross annual salary starting at 70,100
  • opportunity to work with a single client
  • career development in a global clinical research organization

Verantwortungsbereiche

  • Prepare and contribute to high-level budget estimates and detailed proposals
  • Oversee contract management, ESP contracts, and change orders to ensure service delivery per contract
  • Act as primary country-level contact and monitor project progress and enrollment targets
  • Maintain trial management systems and generate reports to track progress
  • Support HA inspections and internal QA audits
  • Contribute to site-level recruitment strategy and contingency planning
  • Deliver vendor management at country level and support vendor selection
  • Contribute to patient understanding of protocol and country-specific informed consent
  • Ensure AE/SAE/PQC reporting within timelines and proper documentation
  • Maintain Inspection readiness and archiving in CTMS/VTMF
  • Collaborate to implement CAPA for audits/inspections
  • Ensure accurate financial reporting and budget adherence; forecast and manage country/local budget
  • Assist in negotiation of site contracts and budgets if applicable
  • Ensure regulatory approvals (IEC/HA) as applicable
  • Mentor or represent functional area in process initiatives if applicable

Zentrale Anforderungen

  • Master in Life Science
  • Minimum 5 years of clinical research experience in pharma/CRO plus 1–3 years local trial management
  • Therapeutic expertise in Oncology
  • Strong knowledge of GCP/ICH and regulatory requirements
  • Fluent German (C1) and good English
  • Strong IT skills and proficiency with company systems
  • Excellent decision-making and financial management abilities
  • Ability to manage study teams in a virtual environment
  • Willingness to travel occasionally
  • strong decision-making
  • financial acumen
  • flexibility
  • CTMS
  • VTMF
  • budgeting and contract management

Local Trial Manager - Sponsor Dedicated Arbeitgeber: IQVIA

IQVIA ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern in New Orleans die Möglichkeit bietet, in einem dynamischen und unterstützenden Umfeld zu arbeiten. Mit einem starken Fokus auf berufliche Weiterentwicklung und einem flexiblen Arbeitsmodell fördert das Unternehmen eine positive Work-Life-Balance und ermöglicht es den Flex Nurse Educators, Patienten durch innovative Bildungsansätze zu unterstützen. Die Unternehmenskultur legt Wert auf Teamarbeit und Vielfalt, was IQVIA zu einem attraktiven Arbeitsplatz für engagierte Fachkräfte macht.

I

Kontaktdaten:

IQVIA Recruiting-Team