
Senior Director, Program Management
Parabilis Medicines
full-time
Posted on:
Location Type: Remote
Location: Massachusetts • United States
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Salary
💰 $260,000 - $300,000 per year
Job Level
Tech Stack
About the role
- oversee the planning, execution and delivery of early and mainly late-stage oncology programs
- ensure that projects align with our strategic objectives and are completed on time and within budget
- coordinate cross-functional teams with the Global Project Team (GPT)
- drive project strategy in coordination with the Program Development Team Leader (PDTL)
- foster communication across the organization
- assist the GPT to build and maintain the Integrated Development Strategy Plan and its integrated timelines
- track progress against milestones
- integrate cross-functional data to help inform decision making
- ensure cross-functional awareness and readiness for key activities
- identify and mitigate project risks proactively
- developing contingency plans to address potential challenges and ensure project success
- escalate critical issues with options and team recommendations
- assist in managing program budgets and budget forecasting
- partner with regulatory team to prepare Health Authorities meetings and submission planning and execution
- coordinate with the GPT to prepare material for governance committees
- summarize actions, decisions and ensure follow-up
- collaborate with key stakeholders across various functions, including clinical development, clinical operations, regulatory affairs, CMC, finance, commercial, and quality assurance
- establish key performance indicators (KPIs) and metrics to monitor project progress
Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field required; advanced degree (e.g., MBA, PhD) preferred.
- 12+ years of project management experience in the biopharmaceutical industry, with a minimum of 5 years in a leadership role focused on oncology drug development.
- Proven track record of successfully managing complex oncology projects through all phases of development, including preclinical and clinical trials.
- Strong understanding of regulatory requirements and industry standards related to drug development and commercialization.
- Exceptional leadership, communication, and interpersonal skills, with the ability to influence and engage senior stakeholders and cross-functional teams.
- Demonstrated ability to think strategically and translate strategies into actionable plans.
- Proficient in project management methodologies and tools (e.g., MS Project, Asana, Trello); PMP or equivalent certification is preferred.
- Strong analytical and problem-solving skills, with a focus on achieving results in a fast-paced environment.
- Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.
Benefits
- an annual target bonus
- equity
- a comprehensive suite of competitive benefits designed to support our employees’ overall well-being
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
project managementoncology drug developmentregulatory requirementsclinical trialsbudget forecastingKPI establishmentstrategic planningrisk managementdata integrationanalytical skills
Soft Skills
leadershipcommunicationinterpersonal skillsstrategic thinkinginfluencingcollaborationproblem-solvingdecision makingstakeholder engagementcross-functional coordination
Certifications
PMP