Real World Evidence Study Manager (Italy)

Real World Evidence Study Manager (Italy) page is loaded Real World Evidence Study Manager (Italy) Apply locations Parma, Emilia Romagna time type Full time posted on Posted 19 Days Ago job requisition id R1405528

Our client, Chiesi Farmaceutici – one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of a Real World Evidence (RWE) Study Manager who can join an exciting working environment in a dynamic and international atmosphere.

RESPONSIBILITIES:

Strategy

• Supports the strategy definition and implementation of RWE studies based on secondary data analysis, and other RWE assigned projects, in order to contributes the achievement of Chiesi strategic goals and medical/scientific standards under RWE Program Leader guidance
• Actuate and consolidate the communication strategy involving all relevant stakeholders on the progress of the RWE projects cross-functionally in the Company

Global Studies

• Coordinates the RWE study teams in the selection, verification and supervision of the CRO and other providers (related to activation, management and performance monitoring), pursuant to the terms of the legislation GCP, GVP and other local legislation applicable.
• Oversights the management of the RWE secondary data collection studies/initiatives
• Contributes to relevant RWE publications in the area of competence when needed
• Checks monthly costs invoiced to Chiesi based on planned study activities vs actual.

Processes and tools

• Support the implementation and specific adaptation of procedures within RWE studies fulfil regulatory requirements and company strategic goals.

REQUIREMENTS AND SKILLS:

• Experienced in team management and propension for team work
• Experienced of principles of clinical study design, planning tools and planning principles
• Experience of ICH/GCP and company SOPs
• Knowledge of budget planning and administrative management with specific SAP tool knowledge

• Experienced in documental archiving and management
• Proficient written and spoken English
• Problem solving
• ime Management
• Quality Orientation
• Stress Management
• Planning & Organizing
• Project Management
• Responsiveness
• Team Working
• Conflict’ Management

TYPE OF CONTRACT:

Permanent contract

IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.903/77).

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

About Us

IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us. #J-18808-Ljbffr