Senior Director, Specialty Project Management
Company: CSL
Location: King of Prussia
Posted on: March 19, 2026
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Job Description:
Oversees Specialty Project Managers(PMs) supporting regional
R&D execution (China &Japan), Submissions, and Search & Due
Diligence across a portfolio of assets ranging from early research
to late-stage development and lifecycle management focusing on all
elements of Project Management Leadership, both strategic and
operational, associated with R&D Program Management. This role
oversees Development Planning & Project Management for China PM,
Japan PM (indirect), Submissions PM and Search & Due Diligence PM.
Manages a distributed team across multiple time zones and cultures,
influences senior cross-functional leaders, and enables high-stakes
decisions that impact patient safety, regulatory approvals, and
business investment. Main Responsibilities & Accountabilities
R&D Specialty Program Management • Accountable for providing
Program Management leadership within the Specialty portfolio and
across geographies, including New Product Development and Life
Cycle Management• Lead the Specialty Project Management function
within R&D Portfolio & Operations Excellence, setting strategy
and operating model for complex, cross-functional programs that
include regional execution (China & Japan), regulatory submission
delivery, and Search & Due Diligence/Business Development
evaluations. • Establish clear role definitions, governance, and
ways of working across Specialty PM areas and regions to ensure
consistent delivery standards and decision-making cadence.• Ensure
all programs and submissions under Specialty PM oversight adhere to
internal quality systems, compliance expectations, and
documentation standards. • Embed risk management discipline: early
detection, mitigation plans, and escalation pathways, including
proactive compliance considerations for China & Japan.• Serve as a
senior PM thought leader, advising R&D and functional leaders
on program strategy, sequencing, trade-offs, and execution risk
across the development lifecycle for the Specialty projects.• Lead
identification of project acceleration and risk management options,
while ensuring solutions are pragmatic and flexible to allow for
innovation• Actively contribute as a member of PPE Leadership Team
to enable success of the group and create a culture of
connectivity, delivery, empowerment and transformation• Provide
guidance and direction to the R&D Specialty Project Management
teams to ensure robust, yet pragmatic, Project Management practices
and methodologies are applied and aligned with broader R&D
projects within our portfolio• Liaise with the TA Delivery Leads to
ensure that processes and delivery outcomes are aligned across the
Therapeutic Areas (TA) and Specialty Project Management• Ensure
seamless interactions between Specialty PM and critical partners
(i.e. TALTs, GPLs, PMs, RPLs, PSTs and functional representatives)•
Contribute to the development of cross functional TA strategy and
process to ensure product strategy plans align with the TA strategy
• Works with Portfolio Management team to ensure Specialty
portfolio information is effectively integrated into portfolio
plans and analysis to support TA portfolio investment management
and the development of TA strategic priorities • Works with the
TALT and Portfolio Delivery Leads to review projects in the
portfolio including timelines, cost and resources Regional PM
Leadership (China & Japan) • Directly manage China PMs and work
closely with the Head, R&D Japan (dual reporting model) to
develop regional Project Managers supporting R&D work in China
and Japan, ensuring alignment with global program strategies and
local requirements.• Integrate China/Japan PM planning into global
integrated development plans (IDPs) and timelines, ensuring
seamless handoffs and transparency across regions.• Drive
consistent use of tools, templates, and standards across regions
and cultures while enabling locally optimized execution and
stakeholder management.• Build strong partnerships with local
R&D leadership, Clinical Operations, Regulatory, Quality,
Medical Affairs, Commercial Operations, and external partners to
remove barriers to project delivery. Submissions PM Leadership •
Lead Submissions PM capability across R&D, ensuring robust
planning and execution for key submissions (e.g., IND/CTA,
NDA/BLA/MAA variations, lifecycle submissions) including end-to-end
submission planning and execution, including authoring, review,
publishing, and submission readiness.• Ensure submission plans are
inspection-ready, traceable, and aligned to global regulatory
strategy, including milestone discipline, authoring readiness, and
contingency plans.• Coordinate cross-functional submission
governance including Regulatory Affairs, Clinical, Biostats,
Medical Writing, CMC, Safety, Quality, Labelling, and Publishing.
Search & Due Diligence (S&DD) Project Management Leadership •
Lead S&DD PM to deliver high-quality diligence planning and
execution for internal pipeline opportunities, licensing,
acquisitions, collaborations, and external innovation evaluations.•
Work closely with the Search function and the Search and Due
Diligence (DD) PM supports R&D and Commercial NPO due diligence
activities • Create standardized diligence workplans, functional
request workflows, and executive readouts to enable fast, rigorous
decision-making.• Coordinate diligence activities across R&D,
Regulatory, CMC, Safety, IP/Legal, Finance, Commercial, and
external parties while ensuring confidentiality and clean-team
requirements (where applicable). Talent/Management Responsibilities
& Accountabilities • Lead a global group of PMs with a set of
high-complexity and interfaces; requires oversight of global
sub-functions, with individual strategies and objectives• Establish
strategic priorities, competency framework and performance
expectations designed to support and develop talent to excel and
grow professionally• Lead and manage Specialty PM workforce
planning: capacity, capability mix, sourcing strategy
(FTE/contract), and succession planning. • Build PM capability
through coaching, mentoring, performance management, and targeted
development plans, including region-specific talent strategies for
China & Japan.• Build and sustain deep expertise in regional PM,
submissions PM and diligence PM as specialized capabilities.•
Champion training pathways for submissions PM and Search & DD PM
specialization, ensuring consistent competency progression.
Qualifications & Experience Requirements • Undergraduate
science/business degree in relevant discipline essential,
preferably with post-graduate qualifications• Post-graduate
qualifications in finance, business administration or related field
preferable • 10 years pharmaceutical or biotech experience
inclusive of demonstrated strong Portfolio Management, Project
Management and Team Leadership expertise• Leadership experience in
drug development in China and Japan, submissions and/or Search &
Due Diligence PM• Excellent communication skills (written, verbal,
presentation) in English; experience adapting messaging to suit the
intended audiences• Excellent Strategic Thinking skills• Executive
presence and negotiation skills; Ability to effectively engage
across the enterprise, building constructive relationships to
execute deliverables. About CSL Behring CSL Behring is a global
biotherapeutics leader driven by our promise to save lives. Focused
on serving patients’ needs by using the latest technologies, we
discover, develop and deliver innovative therapies for people
living with conditions in the immunology, hematology,
cardiovascular and metabolic, respiratory, and transplant
therapeutic areas. We use three strategic scientific platforms of
plasma fractionation, recombinant protein technology, and cell and
gene therapy to support continued innovation and continually refine
ways in which products can address unmet medical needs and help
patients lead full lives. CSL Behring operates one of the world’s
largest plasma collection networks, CSL Plasma. Our parent company,
CSL, headquartered in Melbourne, Australia, employs 32,000 people,
and delivers its lifesaving therapies to people in more than 100
countries. To learn more about CSL, CSL Behring, CSL Seqirus and
CSL Vifor visit https://www.csl.com/ and CSL Plasma at
https://www.cslplasma.com/ . Our Benefits For more information on
CSL benefits visit How CSL Supports Your Well-being | CSL . You
Belong at CSL At CSL, Inclusion and Belonging is at the core of our
mission and who we are. It fuels our innovation day in and day out.
By celebrating our differences and creating a culture of curiosity
and empathy, we are able to better understand and connect with our
patients and donors, foster strong relationships with our
stakeholders, and sustain a diverse workforce that will move our
company and industry into the future. To learn more about inclusion
and belonging visit
https://www.csl.com/careers/inclusion-and-belonging Equal
Opportunity Employer CSL is an Equal Opportunity Employer. If you
are an individual with a disability and need a reasonable
accommodation for any part of the application process, please visit
https://www.csl.com/accessibility-statement .
Keywords: CSL, New Rochelle , Senior Director, Specialty Project Management, Energy / Utilities , King of Prussia, New York