Why Patients Need You

Technology impacts everything we do. Pfizer’s digital and ‘data first’ strategy focuses on implementing impactful and innovative technology solutions across all functions from research to manufacturing. Whether you are digitizing drug discovery and development, identifying solutions, or making our work easier and faster, you will be making a difference to countless lives.

What You Will Achieve

Global Product Development (GPD) supports clinical development across Pfizer and late-stage development of medicines. Every year, GPD partners with thousands of global participants, health systems and HCPs in our work to bring new medicines to market for the patients that we serve.

This role will support Clinical Development and Operations (CD&O) and their functional line partners including but not limited to Data Monitoring and Management (DMM), Statistical Programming & Analysis (SPA), Patient Technologies, and Global Site Support, to deliver integrated process, technology and information solutions for clinical trials

This position sits on the Clinical Trial Solutions Team within Information Management. Individuals filling the position listed are responsible for providing leadership to the Greece based Clinical Trial Solutions (CTS) team (colleagues and contractors). Incumbent will partner with the Global CTS Teams to ensure timely solution(s) business support, services, data analysis and data quality services.

How You Will Achieve It

• Liaise with business and technical groups to gather business requirements, define new business processes and support/services, and improve existing processes.
• Accountable for all aspects of the operations of the CTS Greece Team
• Accountable for quality deliverables for all teams managed in the Greece team
• Accountable for managing the vendor relationship for any contracted/outsourced projects in region
• Develop and implement a quality plan to ensure deliverables produced in Greece meet quality standards. 
• Collaborate and Lead discussions with Global CTS Teams to drive innovation and continuous improvements of business processes, solutions and engagement
• Liaise with HR Greece on recruitment, performance management and compensation activities. 
• Develop strategy for retaining colleagues to identify career development opportunities.
• Ensure all activities comply with IM procedures, global regulatory requirements and SOPs
• Coaching, mentoring and developing direct reports and team members
• Complete training in accordance with Information Management curriculum, including Information Protection Management Guidelines (IPMG) and 21 CFR Part 11 training requirements.
• Work within a global team in a matrix environment

Qualifications

BASIC QUALIFICATIONS

• BSc in Computer Science, Life Sciences, Business, engineering, statistics or a related healthcare discipline 
• 5-8 years industry experience in (or supporting) any of the following disciplines: clinical drug development, clinical trial management, safety surveillance and reporting, clinical project management, R&D or. Related experience in other industries will be considered.
• Excellent analytical skills with demonstrated ability to investigate and solve problems
• Knowledge of application system management and change control processes, application validation and implementation in a GxP environment.
• Demonstrated customer relationship skills and capabilities to collaborate with teams.
• Experience working with international colleagues, with skills to understand and present the "big picture" in terms of potential implications
• Ability to communicate complex information and analyses to a variety of audiences in both verbal and written format

Nice-to-Have

• Master's degree and relevant pharmaceutical experience
• Good knowledge of System Application & Products and core solutions deployed at the site

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