Senior Director, Project Management
Current
Jun 2022 - Present
AeroLeads people directory · profile
Maureen Dillon Email & Phone Number
Program Management | Clinical Development | Project Management Professional (PMP)
at
Jnana Therapeutics
1 work email found
@jnanatx.com
LinkedIn matched
✓ Verified July 2026
4 data sources
Profile completeness 100%
Current company
Role
Program Management | Clinical Development | Project Management Professional (PMP)
Location
United States
Who is Maureen Dillon? Overview
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Quick answer
Maureen Dillon is listed as Program Management | Clinical Development | Project Management Professional (PMP) at Jnana Therapeutics, based in United States. AeroLeads shows a work email signal at jnanatx.com and a matched LinkedIn profile for Maureen Dillon.
Maureen Dillon previously worked as Senior Director, Project Management at Jnana Therapeutics and Senior Director, Program Management, Clinical Development at Agios Pharmaceuticals. Maureen Dillon holds Masters, Business Administration from Babson College.
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{first_initial}{last}@jnanatx.com
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Profile bio
About Maureen Dillon
I am an experienced professional focusing on the areas of program management, development and growth management within the biopharmaceutical industry. This includes collaboratively creating and driving program strategy and guiding cross-functional teams through the full development lifecycle in rare diseases, metabolic disorders, and oncology. I have also partnered with many functional heads to help design and lead numerous initiatives to support quality assurance and growth/restructuring of departments and systems. DEVELOPMENT: - Early and Late-Stage (Phase 1-4) - Target Product Profiles (TPPs) - Integrated Development Plans - IND/NDA/MAA Submissions - Pediatric Plans - Rare Disease / Oncology / Metabolic DisordersPROGRAM MANAGEMENT: - Budgets / Resources - Goals / Long-Range Plans - Risk Identification / Mitigation - Stakeholder Alignment - Stage-Gate Preparation/Reviews - Partnership CollaborationGROWTH MANAGEMENT: - Process Development/Optimization - Governance Development - Decision Making Mapping - Line Management / Hiring - MentoringKEY ACCOMPLISHMENTS:-Managed teams in the preparation of 3 IND submissions, 5 US NDAs, 2 MAAs and several rest of world filings including China NDA-Oversaw transition of development teams during acquisitions, mergers, divestiture and joint venture while maintaining timelines and key resources-Built development project management function at multiple companies including identifying needs, developing tools, and hiring/managing group-Developed and implemented new LRP/budget process to increase accuracy and transparency resulting in more robust budget and resource projections-Created and administered development governance process that resulted in timely and documented alignment between team and senior management -Collaborated with colleagues to create job descriptions/competencies, escalation procedures, and redesign of global integrated development plan template resulting in improved consistency and an ease of use for senior management-Managed clinical development systems-based projects balancing requirements from IT, Quality and various clinical development functions including implementing Argus safety database on time and within budget-Collaborated with functional experts to simplify internal standard operating procedures with the goal of decreasing resource needs and lead times -Partnered with human resources to develop and run team building activities to strengthen both development and leadership teams
Listed skills include Biotechnology, Clinical Development, Fda, Cross Functional Team Leadership, and 19 others.
Current workplace
Maureen Dillon's current company
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5 roles · 36 years
Maureen Dillon work experience
A career timeline built from the work history available for this profile.
Senior Director, Program Management, Clinical Development
Created and led new clinical development program management function to support cross-functional clinical development teams for rare disease and oncology. In collaboration with therapeutic area leads, defined governance review timing and content, prioritized program resources, escalated key issues and risks, and ensured timely decision making and clear communication to maintain organization-wide alignment.Partnered with program leads, functional leads, and financial planning representatives to define and track changes to clinical development 5-year plan and annual goals. Identified critical path and key milestone dates to ensure consistent assumptions for resource and expense planning for complex, global programs including major regulatory filings. Represented project management on clinical leadership team responsible for reviewing operational metrics, resource needs and change management for clinical development organization.Administered clinical development organization meetings including governance committee, leadership team, staff, and systems meeting forums.
Mar 2016 - Nov 2021
Project Leader / Senior Director Clinical Research
Project Leader / Senior Director, Clinical Research (2005-Present)Project Leader / Director Clinical Research (2000-05)Lead global development teams in defining development strategy and executing plans for global clinical studies (phase 2, phase 3 and post marketing) and regulatory marketing approvals worldwide (2 NDAs, 2 MAAs, China NDA) for full product lifecycle including line extensions. Lead global teams in preparation of 2 Investigational New Drug (IND) submissions and presented at successful pre-IND meeting. Evaluated multiple external product opportunities and led multifunctional research and development discussions with prospective partners resulting in clear, integrated company position.
Jan 2000 - Jul 2015
Associate Director, Clinical Research
Geltex Pharmaceuticals (Acquired By Genzyme)
Associate Director, Clinical Research (1998-00)Assistant Director, Clinical Research (1997-98)Manager, Clinical Research (1996-97)Directed and integrated efforts of multiple contract research organizations (CROs) to analyze and report phase 2 and 3 studies and integrated safety summary analysis to support filings. Oversaw clinical NDA/MAA sections and defended applications for FDA/EMA approvals.Designed and implemented high-profile outcomes study leveraging 3 site management organizations and 2 CROs completing enrollment of 2000 patients in 10 months.
1996 - 2000
~4 yrs
Manager, Operations
Boston Biostatistics (Acquired By Icon)
Manager, Operations (1993-96)Project Manager (1992-93)Masters Level Statistician (1991-92)
1991 - 1996
~5 yrs
3 education records
Maureen Dillon education
Masters, Business Administration
Babson College
Bachelor Of Arts, Mathematics
Boston University
Master Of Arts, Mathematics (Statistics)
Boston University
FAQ
Frequently asked questions about Maureen Dillon
Quick answers generated from the profile data available on this page.
What company does Maureen Dillon work for?
Maureen Dillon works for Jnana Therapeutics.
What is Maureen Dillon's role at Jnana Therapeutics?
Maureen Dillon is listed as Program Management | Clinical Development | Project Management Professional (PMP) at Jnana Therapeutics.
What is Maureen Dillon's email address?
AeroLeads has found 1 work email signal at @jnanatx.com for Maureen Dillon at Jnana Therapeutics.
Where is Maureen Dillon based?
Maureen Dillon is based in United States while working with Jnana Therapeutics.
What companies has Maureen Dillon worked for?
Maureen Dillon has worked for Jnana Therapeutics, Agios Pharmaceuticals, Sanofi Genzyme, Geltex Pharmaceuticals (Acquired By Genzyme), and Boston Biostatistics (Acquired By Icon).
How can I contact Maureen Dillon?
You can use AeroLeads to view verified contact signals for Maureen Dillon at Jnana Therapeutics, including work email, phone, and LinkedIn data when available.
What schools did Maureen Dillon attend?
Maureen Dillon holds Masters, Business Administration from Babson College.
What skills is Maureen Dillon known for?
Maureen Dillon is listed with skills including Biotechnology, Clinical Development, Fda, Cross Functional Team Leadership, Medical Writing, Clinical Research, Pharmaceutical Industry, and Clinical Trials.
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