Manager Business Analyst

2 weeks ago

Kirkland, Canada Pfizer Full time

Posting closing date: February 22, 2023- Date de fin d’affichage : le 22 février 2023- Status : Regular, Full-Time- Statut : Régulier, temps pleinRole Summary

As part of an agile team, will lead the ideation, strategy and development of information management solutions for the Regulatory domain; use business analysis skills and domain knowledge to elicit requirements and drive timely decisions to achieve desired business outcomes, and work across Global Regulatory, other Regulatory partner lines (e.g. Safety, Manufacturing, Pharmaceutical Sciences and Digital) to execute projects that deliver robust solutions for regulatory affairs.

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.-
- Coordinate user testing and acceptance of information solutions prior to deployment.- 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.- Experience in building/managing solutions in one or more areas of Regulatory Intelligence and Policy, Chemistry and Manufacturing Controls, Submissions Management, Publishing, and Labeling.

TECHNICAL SKILL REQUIREMENTS- Experience with regulated systems used in pharmaceutical industry or other GxP area.-
- Knowledge of healthcare and/or pharmaceutical metadata and standards.

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

Pre-employment requirement:

- Be fully vaccinated against COVID-19*
- Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies that is at the forefront of the fight against COVID-19, Pfizer is proud to declare that it expects its employees to be fully vaccinated. Fully vaccinated is defined as receiving the full dose therapy of a Health Canada approved COVID-19 vaccine at least 14 days post the completion of the required dose regimen.

We are proud to offer employees a flexible working model that is grounded on empowering colleagues to design their workdays so that they can maximize their productivity, enhance their work-life balance and support a way of working that fosters innovation and patient-centricity. Currently, our employees are expected to be on-site 2-3 days per week blending on-site collaboration and connection with off-site remote working when it makes business sense to do so.
- Chef, analyste de l’information commerciale

Résumé du poste

Au sein d’une équipe agile, le titulaire de ce poste dirigera la création et le développement de solutions de gestion de l’information ainsi que les stratégies liées à celle-ci pour le secteur des Affaires réglementaires; ses compétences en analyse commerciale et ses connaissances du domaine seront mises à profit pour déterminer les exigences et prendre des décisions opportunes afin d’atteindre les résultats d’entreprise souhaités. Il travaillera au sein des Affaires réglementaires à l’éc

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