Content Enablement Sr Associate – Italy (12 Mesi Somministrazione)

This role will contribute to Content Enablement service delivery activities within Italy that allow the business to drive quality at scale.

The Content Enablement – Italy (Sr. Associate) role will work under supervision with the Content Enablement team, other Biopharma Ops Leads, and Biopharma Ops Partners (BOPs) to operationalize key global Content Enablement services in Italy such as content curation and production, Review and Approval and Policy Management, and material logistics management.

Key Attributes

Accountable for contributing as a team member to deliver the Content Enablement remit within Italy while enhancing service delivery continuity and quality.

Responsible for applying technical knowledge to support delivery of the below Content Enablement activities in Italy:

• Content Supply Chain Management (GCMA, Review & Approval Processes, and Policy/Addendum Management)

• Content curation and production (CANVAS and Content Factory Services)

• Materials Management (Logistics & warehousing)

Uses established processes and guidance from colleagues on the team to deliver strategic solutions that advance and optimize Content Enablement activities under a globally connected, locally-embedded model. Reports to the Content Enablement Lead – All EU.

This role will be a key member of the Content Enablement – All EU team.

ROLE RESPONSIBILITIES

• Supports the compliant review, approval & build of Pfizer Content through using Enterprise Policy, Procedure/Addendum, and Process Support tools (e.g., Veeva Vault)

• Works closely with brand marketing and marketing enablement teams to ensure content is effectively reviewed and deployed

• Train Italy users on content curation & CANVAS tools

• Monitor content approval & publishing and in general supporting each phase of the content lifecycle management, ensuring compliance

• Take responsibility for assigned portion of the Content Enablement team’s milestones/ deliverables. Supports the usage of Biopharma Ops service delivery tools and platforms. Improves quality, consistency (One Pfizer), and compliance across BUs and Italy.

• Facilitates interactions between marketing teams and Content Factory – including content demand management.

• Key member of the Future of Content (FOC) team in Italy and supports in the ongoing improvement of the E2E content creation process

• Engages with Biopharma Ops Partners (BOPs) and BU Leads to understand and 1) ensure alignment of Biopharma Ops’ client strategies in Italy and 2) determine optimal resource allocation and investment that enables efficient and high-quality HCP engagement

PREFERRED QUALIFICATIONS

• BA Required 3+ years of commercial experience, preferably in brand marketing or operations in Italy

• Cross-BU and/or diversity of job experiences

• Solid knowledge of Veeva Vault

• Solid knowledge of global/local content policies

• Experience with FOC process

• Solid knowledge of excel to execute ad hoc analysis upon request

• Experience in project management

• Excellent communication skills

• Proven track record of contributing to the completion of project tasks and/or milestones

• Knowledge of pharmaceutical market and relative business levers together with regulatory/compliance aspects

• Possesses a deep understanding of business landscape in Italy and BU strategies to determine key priorities and their impact on Content Enablement activities

• Ability to process unstructured data sources and produce structured reports

• Demonstrated agility and ability to drive program completion under supervision in expedited timelines

• Previous experience in communication/advertising agencies is not mandatory but very much appreciated

Expect candidates to demonstrate these personal competencies:

• Courage, Excellence, Equity, Joy

• Italian mother tongue

• Fluent English is a must

• Results orientation

• Teamwork oriented

• Willing to grow professionally

LAST DAY TO APPLY: DECEMBER 7th 2022

THIS IS A 12 MONTH CONTRACT (SOMMINISTRAZIONE)

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