Dr. Ina Raudonat

Berufserfahrung von Ina Raudonat

• Bis heute 3 Jahre und 9 Monate, seit Okt. 2020

  Senior Clinical Project Delivery Manager

  Labcorp - Fortrea Germany GmbH

  Global oversight of clinical delivery within the portfolio in oncology and biopharma for key clients. Contributed to client proposals and budget generation to support business growth. Support of Clinical Study Manager based in EMEA and Canada during audits and inspections with focus on CAPA Management. Proactively lead both quality control and risk management activities to ensure project deliverables are met. Ensuring KPIs are within scope of contract.

• 1 Jahr und 9 Monate, Jan. 2019 - Sep. 2020

  Senior Manager Clinical Operations

  Covance Clinical Development GmbH

  Supported the maximization of the profitability of operations in assigned countries ensuring that all deliverables are met on time. Performed detailed review of billable hours and associated utilization per assigned objectives and take action as appropriate. Drove department resourcing strategy ensuring the right talent are assigned to the right projects at the right time; ensure that the talent is fully utilized.

• 1 Jahr und 4 Monate, Sep. 2017 - Dez. 2018

  Director Clinical Team Leader

  Covance Clinical Development GmbH

  Close Monitoring of financial overburn related to biopharma studies within the Clinical Team Leader Department across EMEA region. Contributed to newly generated RACI to be implemented across the departments. Provided input to relevant SOPs and standard plans/templates for use by Project Management and Clinical Study Managers. Hold Clinical Study Managers accountable for quality and compliance with SOPs, monitoring visit cycles, trip report quality, audit and inspection readiness.

• 1 Jahr und 8 Monate, Jan. 2016 - Aug. 2017

  Director Clinical Team Leader

  Chiltern International Ltd

  Supported a culture of clinical project management excellence in which Clinical Study Manager are effective and have a deep understanding of their role and responsibilities. Sharing knowledge and experience with Clinical Study Managers including leading training sessions within biopharma Clinical Team Leader Department. Hold Clinical Study Manager accountable for GCP issue escalation to management team, sponsor and QA, and determine regional implications for corrective action plans.