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Job Description

Project Planning and Execution: Oversee contracting activities in support of project execution. Develop detailed project plans, including timelines, budgets, and resource allocation. Ensure projects are completed on time and within budget.

Portfolio Management: Support a portfolio of projects within Pfizer's Companion Diagnostic Development Oncology group. Coordinate multiple projects simultaneously, ensuring alignment with overall strategic goals.

Cross-Functional Collaboration: Work closely with clinical development, regulatory affairs, commercial teams, testing labs and external diagnostic partners to align on project goals and strategies.

Regulatory Compliance: Ensure that all companion diagnostic development activities comply with global regulatory requirements. Support the timely preparation of necessary documentation for regulatory approvals.

Risk Management: Identify potential risks and develop mitigation strategies. Monitor project progress and address any issues that arise.

Stakeholder Communication: Serve as the primary point of contact for internal and external stakeholders as required. Provide regular updates on project status and ensure effective communication across all teams. Ensure deliverables, actions and resolutions are documented and tracked both at the project and portfolio levels through completion.

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) .

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Skills and Requirements

5+ years of project or program management experience

Bachelor's degree or higher [degree can be flexible with additional experience]

Extensive Excel knowledge

Proven experience working on complex projects

Excellent communication, organization, and problem solving skills Experience in Power BI dashboard creation and basic Sharepoint development

Project management experience within a clinical trial or CRO (Contract Research Organization) group

Companion diagnostics (CDx) experience

In Vitro Diagnostics (IVD) experience null

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].