Senior Product Manager
Company | Exact Sciences |
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Location | Madison, WI, USA, San Diego, CA, USA |
Salary | $129000 – $208000 |
Type | Full-Time |
Degrees | Bachelor’s, MBA, PhD |
Experience Level | Senior, Expert or higher |
Requirements
- Master’s degree in business administration, scientific, or related field; or Bachelor’s degree in business administration, scientific, or related field and 2 years of relevant experience in lieu of Master’s degree.
- 5+ years of experience working in a team setting in healthcare product development and/or commercialization with a demonstrated ability to effectively contribute toward team goals.
- 5+ years of experience in a regulated environment (including CLIA, FDA, CE, IVDR).
- Proficient in Microsoft Office Excel, Word, and PowerPoint.
- Demonstrated ability to perform the essential duties of the position with or without accommodation.
- Authorization to work in the United States without sponsorship.
Responsibilities
- Maintain overall accountability for project success in securing and marshalling the people, budget, and other resources required to execute program objectives.
- Represent the project and project team to the Screening Business Unit.
- Help clear barriers to team progress and resolve conflicts within the team and outside of the team.
- Delegate effectively to other functions who may or may not be direct reports.
- Maximize the value of Exact Sciences’ Pipeline programs by developing and maintaining a portfolio of projects that support the long-term strategy and business plan for the product.
- Contribute to development and execution of the product strategy.
- Provide project leadership with deep interactions and collaboration with R&D scientists, Commercial, Clinical Development, Lab Operations, Market Access, Regulatory, Business Development, and product lifecycle management colleagues.
- Develop and deliver compelling presentations to convey program strategies and/or facilitate key decisions to a broad set of stakeholders including senior leaders.
- Apply knowledge of product development processes and deliverables in regulated environments (FDA, ISO, CE/IVDR).
- Promote an open, collaborative environment built on trust to foster positive teamwork.
- Exceptional communication skills including oral, written, and presentation techniques.
- Self-starter with the ability to prioritize and drive to results with a high emphasis on quality.
- Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
- Support and comply with the company’s Quality Management System policies and procedures.
- Maintain regular and reliable attendance.
- Ability to act with an inclusion mindset and model these behaviors for the organization.
- Ability to work nights and/or weekends, as needed.
- Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
- Ability to travel 30% of working time away from work location, may include overnight/weekend and international travel.
Preferred Qualifications
- PhD in life sciences, business, or related field.
- 7+ years of experience working in a team setting in healthcare product development and/or commercialization.
- Strong analytical skills for financial modeling or data analysis.
- Experience with development and commercialization of products outside of the United States.
- Experience with working in both the clinical environment (i.e., with health care providers) and the molecular diagnostic lab environment (qPCR and NGS experience a plus).
- Strong knowledge and experience in cancer screening and oncology.