Senior Associate Information Management

3 weeks ago


Remote, United Kingdom Pfizer Full time

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.

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.

What You Will Achieve

This position sits on the Clinical Trial Solutions Team within Information Management. This role will support Clinical Development and Operations (CD&O) and their functional line partners including 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

As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It
- Work closely with functional lines to articulate business needs for new solutions or changes to existing solutions.
- Document options and proposals for solution governance on how best to meet customer needs.
- Document business requirements for IM solutions. Participate in workshops, conduct interviews with functional line SMEs to ensure full and complete requirements set. Ensure endorsement from functional lines.
- Collaborate with functional lines to understand and document the use of the information management solutions with the business process.
- Coordinate user testing and acceptance of information solutions prior to deployment.
- Work with business stakeholders to listen to their needs and articulate into projects and provide ongoing status on progress of key projects.
- Contribute to solution road maps.
- Contribute to continuous improvement projects to simplify and improve system use and system management.
- Collaborate with functional lines to ensure a consistent approach with business process-specific training.
- Gather metrics and generate standard reports regarding usage or support of IM systems
- 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**:
Must-Have
- Moderate pharmaceutical 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 regulatory reporting and analytics, or regulatory affairs. Related experience in other industries will be considered.
- Demonstrated analytical skills with demonstrated ability to investigate and solve complex problems.
- Strong project management and organizational skills.
- Ability to interface with international colleagues, understand the “big picture” in terms of potential implications of changes to systems and processes to sites and/or affiliates outside of home country/region.
- Ability to interact in a professional manner and build strong collaborative relationships with internal Pfizer teams.
- High School Diploma or equivalent education.
- Understands concepts of information management with emphasis on document and records management.
- Knowledge and experience in project management, data analysis, business analysis, and information integration.
- Demonstrated customer relationship skills and capabilities and collaboration on teams
- Excellent written and verbal communication skills.
- Proficient in English.

Nice-to-Have
- BS/MS in Computer Science, Life Sciences, Business, engineering, statistics or a related healthcare discipline.
- Experience in building/managing solutions in one or more areas of clinical trials including any of the following:

- Trial recruitment, study design, study and site management
- Data management and monitoring
- ePRO/eCOA, Sensors & Wearables, eConsent and Patient Engagement technologies
- Statistical analysis
- An understanding of healthcare and/or biopharmaceutical data and systems.

LI-Remote

Purpose

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itsel



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