Director, Program Management
Company: AVEO Pharmaceuticals
Location: Boston
Posted on: November 14, 2024
Job Description:
Position: Director-level Program Management
Department: Program Management
Reports to: Manoj Patel
Location: Boston
We are looking for an experienced Director of Program Management in
support of Aveo's growing oncology pipeline. This individual will
report directly to the Vice President of Program Management. The
Director, Program Management will have both early and late phase
pharmaceutical program management experience that includes
knowledge of the drug development process and inter-dependencies of
key functions including research, clinical manufacturing,
regulatory and external partners. This individual will also have
demonstrated success in managing programs using best in class
methodologies and software combining strong foundational knowledge
of various segments of the life sciences industry. The ideal
candidate will have strong financial and analytical capabilities,
refined communication skills and the ability to thrive in a
fast-paced, dynamic, and highly collaborative environment.
Key Responsibilities include:
Ownership of the program plans and finances.
- Apply best practices in the development, initiation, planning,
execution, control and closing of projects, and to interact with
all program stakeholders including pre-clinical and clinical
development, business, manufacturing and regulatory departments to
ensure alignment on program goals, timelines, and resources
required.
- Provide program management expertise for project managers and
multiple projects that may include external co-development
partnerships.
- Ensure that cross-functional core team(s) are aligned on goals
and timelines to deliver milestones on or ahead of
schedule.
- Work cohesively with various disciplines to leverage functional
expertise within R&D, Commercial, Clinical, Quality,
Regulatory, Operations, etc., and establishes integrated project
plans and objectives.
- Bridge the gap between strategy and tactical execution at the
project level. This position requires knowledge and experience in
effectively managing project risks, diverse disciplines, cultures,
locations, personalities, communication styles, conflicting
priorities and/or requirements.
- Identify and leverage inter-dependencies in short-, mid-, and
long-term program plans and advise teams on areas of risk or
possibilities to accelerate development.
- Challenge assumptions and provide recommendations to improve
processes and outcomes.
- Create and manages the integration of project schedules and
budgets.
- Resolve resource allocation issues, conflicts, and priorities
to ensure the project is staffed appropriately, completed on time,
and within budget constraints.
- Measure progress, communicates, and escalates proactively
impact of changes (e.g. scope, cross functional resources,
timelines, costs, etc.) to key stakeholders.
- Ensure that the acceptance criteria for system/product level
integration are completely aligned with the design and project
management requirements for integration. Facilitate team process
needed to meet requirements to demonstrate system/product level
integration readiness.
- Ensure the timely collaboration and coordination of design
requirements, cross functional resourcing, and scheduling between
projects, sites, and platforms.
- Deliver presentations at communication and governance meetings
utilizing project dashboards, and messaging.
- Contribute to the functional excellence of project management
by participation in the development and continuous improvement of
processes, procedures, and tools related to program and portfolio
management practices.
- Perform other duties & projects as assigned
Capabilities/Quality
- Continuously enhances personal understanding and application of
program management tools and methodologies in the pharmaceutical
industry and other industries
- Participates in process improvement initiatives and brings in
external perspective and industry standard practices
- Performs project and program level data analyses and reporting,
as needed
- Conducts periodic health checks to ensure quality of project
planning and control.
Basic Qualifications:
- Minimum 5 years pharmaceutical R&D or related industry
experience
- Basic knowledge of multi-disciplinary bio/pharmaceutical drug
development required
- Exceptional computer proficiency - advanced knowledge of and
experience with MS-Office applications (including Word, PowerPoint,
Excel, Smartsheets and Project)
Preferred Qualifications:
- Oncology project management experience a plus
- Experience with biologic drug development and biologic
manufacturing processes a plus
- Strong written and verbal communication skills and EQ
- Undergraduate degree / advanced degree in life science or
business
- Direct experience in bio/pharmaceutical program
planning
- PMP certification
- Strong experience with Planisware and/or MS Project
- Background in risk, budget, and resource management
- Ability to effectively manage multiple projects and
stakeholders with competing priorities.
AVEO Oncology ("AVEO") is an oncology-focused biopharmaceutical
company committed to providing innovative solutions to improve
cancer patients lives. On January 20, 2023, AVEO was acquired by LG
Chem, Ltd. ("LG Chem"), establishing a U.S. commercial presence for
LG Chem and expanding LG Chem's global oncology portfolio. AVEO
continues to commercialize FOTIVDA (tivozanib) in the U.S. To learn
more about FOTIVDA efficacy, safety, and relevant resources, visit
.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, disability, or status as a
protected veteran.
Keywords: AVEO Pharmaceuticals, Leominster , Director, Program Management, Executive , Boston, Massachusetts
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