Information Manager, Project Manager

2 weeks ago

Kirkland, Canada Pfizer Full time

Posting closing date: February 21, 2023

Date de fin d’affichage : le 21 Février 2023

Status : Regular, Full-Time

Statut : Régulier, temps plien

ROLE SUMMARY

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 partner with Pfizer Global Product Development, Worldwide Research & Development, Digital and other support functions to ensure timely project execution and delivery.

ROLE RESPONSIBILITIES
- Work closely with functional lines to articulate business needs for new solutions or changes to existing solutions and document business requirements for assigned solutions. Run workshops and conduct interviews with functional line SMEs to understand the business need and then ensure full and complete requirements set. Ensure endorsement from functional lines.
- Document options and proposals for solution governance on how best to meet customer needs.
- 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 key stakeholders to listen to their needs and articulate into projects and provide ongoing status on progress of key projects.
- Collaborate with partners, stakeholders, and team members to manage solution road maps.
- Lead continuous improvement projects to simplify and improve system use and system management.
- Lead medium to large projects, following established methodologies.
- Collaborate with functional lines to ensure a consistent approach with business process-specific training.
- Drive active decision making through pre-existing governance with a complex set of stakeholders.
- Provide direction to junior level team members supporting owned project work and work activities.

BASIC QUALIFICATIONS
- Minimum of 5 years 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 strong analytical skills with ability to investigate and solve unusual and complex problems independently.
- Demonstrated strong customer relationship skills and capabilities to influence and collaborate with teams.
- Proven ability to communicate complex information and analyses to a variety of audiences in both verbal and written format, capable of effectively summarizing abstract concepts into clear, concise, and insightful business cases.
- Proven ability to operate in a fast-paced, high-energy environment and comfort with operating in situations with significant ambiguity.
- Minimum of a bachelor’s degree (BS or BA) with higher academic qualification/degree preferred or equivalent relevant professional experience

PREFERRED QUALIFICATIONS
- MS in Computer Science, Life Sciences, Business, Engineering, Statistics, or a related discipline.

TECHNICAL SKILL REQUIREMENTS
- Experience with regulated systems used in pharmaceutical industry or other GxP area.
- Knowledge of healthcare and/or pharmaceutical metadata and standards.
- Experience with query tools/data extraction techniques (e.g., SQL, PL/SQL, Brio, MS Access) preferred.

REQUIRED APTITUDES
- Action oriented and energetic.
- Resourceful and creative; avid learner.
- Easily makes connections - Quick to establish trust and respect.

DOMAIN COMPETENCIES

Data Aggregation and Reporting

Experience providing data analysis, reporting and building visualizations for solutions across Regulatory, Clinical and Safety Solutions. Understanding of database querying and data system management in order to assist resources with work assignments. Knowledge of SQL, Alteryx, Spotfire recommended.

PHYSICAL/MENTAL REQUIREMENTS

Extensive computer use

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Domestic and International travel of 10-20% (as required)

ORGANIZATIONAL RELATIONSHIPS

Provide the primary groups or key role(s) that this role will have interaction with as a regular part of the role responsibilities. Include any external interactions as appropriate.
- Reports into GPD Information Management organization and collaborates with other IM functions to deliver services.
- Interacts directly with GPD functional line leaders, and other business units including Worldwide Research & Development (WRD).
- Partnerships with support functions, including Digital, Finance, Procurement, Human Resources, Legal, and Quality Assurance.
- External relationships with partner companies
- This description indicates the general nature and level of work expected. It is not des

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