5+ years of experience in program or project management; 7+ years preferred.
Proficiency in project management principles including scope, schedule, resource, and risk management.
Experience leading large-scale product development projects, particularly in international settings.
Familiarity with FDA regulated products and compliance standards.
Responsibilities
Lead projects through the entire management lifecycle, ensuring completion within scope, schedule, and budget.
Identify and mitigate project risks while managing scope changes effectively.
Develop and implement comprehensive project plans covering all critical aspects.
Facilitate team communications and act as a liaison with external biopharma partners.
Build strong relationships with functional leaders to enhance project success.
Benefits
Flexible work arrangements including hybrid options.
Access to comprehensive health and wellness programs.
Opportunities for professional development and advanced training.
Participation in a discretionary annual bonus program.
Commitment to a culture of integrity, courage, and passion.
Full Job Description
About the Job:
The Senior Project Manager, part of the Portfolio and Program Management Team, is responsible for the planning and execution of new biopharma clinical product development projects and/or lab expansion projects, as well as other business critical initiatives. The role manages multiple projects with competing timelines and interfaces with external biopharma partnerships. For each project, the role generates and executes project plans to deliver the defined solution business cases, as well as identifies and resolves resource requirements and issues pertaining to the designated projects. The position develops and manages project deliverables, and the programs and products worked by the incumbent may span from product concept initiation to global commercialization.
Key Responsibilities:
Project Management:
Lead project through the entire project management lifecycle, ensuring all project work is completed according to scope, schedule and budget
Ensures project resources are secured; project resource plans are managed to assure project is not delayed due to resource contention
Project risks are identified, prioritize and mitigated
Manage project scope change management
Develop and implement project plan, including cost, scope, schedule, risk, resource and communications plans.
Build team ownership and commitment to project plans.
Provide structured thinking to project team on overall approach and delegate tasks as appropriate.
Guide the team in appropriate decision-making through analyzing options and reviewing implications with the team. Make decisions pertinent to the project as needed.
Communications and Reviews:
Responsible for team and cross-functional communications (written and oral).
Responsible for project related communications with external biopharma partners (written and oral).
Act as liaison between the project team and FMI governance (Portfolio Governance Committee and the Executive Team) as required.
Define and track key project metrics. Coordinate and guide project phase reviews on metrics.
Elevate critical business decisions to the appropriate committees, management teams or functional managers.
Relationship Management:
Provide input to functional leaders on team and team member performance.
Develop and maintains strong relationships with functional leaders to drive success of projects and teams.
Influence cross-functional collaboration for the purpose of achieving optimal project outcomes.
Develop and maintain strong relationships with external biopharma teams to drive project success.
Process Management:
Facilitate the Project Management Life Cycle (PMLC) at all stages. Derive from the process high quality, high impact deliverables of the project.
Leverage quality system use in project or product creation and continued compliance.
Actively review policy and practices pertinent to designated project for understanding of best practice and functional excellence. Implement improvements on an as needed basis.
Drive efforts to ensure cross-functional systems effectiveness.
Team Management:
Lead a team of cross-functional representatives in the achievement of organizational goals.
Influence in a complex, matrixed environment, for optimal project outcomes.
Foster a team environment that enables all participants to contribute their full potential in pursuit of project objectives.
Monitor and ensure compliance with company policies and procedures (e.g., federal/country and regulatory requirements).
Other duties as assigned.
Comply with FMI's attendance policies
Qualifications:
Basic Qualifications:
Bachelor's Degree
5+ years of work experience in a program or project management role
Preferred Qualifications:
Graduate Degree or advanced project management certification (PgMP, PMP)
7+ years of experience in a program or project management role
Proficiency in program/project management skills and principles, including scope, schedule, resource and risk management
Portfolio of leading international and/or distributed large scale product development projects utilizing project management and product design & development frameworks
Prior experience:
with intercultural teams
using project management tools
involving FDA regulated products
coordinating program details across disciplines and integrate all aspects of business as they impact development projects
with Waterfall and Agile methodologies
working within deadline and resource constraints
managing program scope, roles and responsibilities, specifications, timelines, and resources
in a highly independent position
presenting and communicating with all levels of an organization, as well as with external customers
Effective and clear communication and presentation skills
Demonstrated negotiation and conflict management skills
Willingness to adapt and work in ambiguous and/or changing conditions
Working knowledge of FDA, ISO, CLIA and CAP regulations
Understanding of HIPAA and the importance of patient data privacy
Commitment to reflect FMI's values: Integrity, Courage, and Passion
The expected salary range for this position based on the primary location of Boston, MA is $112,600 - $140,800 per year. The salary range is commensurate with Foundation Medicines compensation practice and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for Foundation Medicine's benefits.
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About Foundation Medicine
Foundation Medicine is a molecular information company dedicated to a transformation in cancer care in which treatment is informed by a deep understanding of the genomic changes that contribute to each patient's unique cancer. The company offers a full suite of comprehensive genomic profiling assays to identify the molecular alterations in a patient's cancer and match them with relevant targeted therapies, immunotherapies and clinical trials. Foundation Medicine was founded in 2010 and is headquartered in Cambridge, Massachusetts.