Director, Project Management Due Diligence

BioSpace; King of Prussia (PA); Hybrid; USD 234,000 - 260,000; Full time

Benefits offered by this job

Hybrid work model

Competitive benefits

Job summary

CSL Behring is seeking a Director of Project Management Due Diligence to lead external-innovation evaluations in a hybrid King of Prussia, PA or Waltham, MA setting. You will supervise integrated plans, budgets, and cross-functional teams across scientific, clinical, regulatory, IP, and commercial domains, driving timely decisions and portfolio growth.

This role emphasizes governance, accountability, and collaboration with senior stakeholders to enable high-quality due diligence and partnership

Qualifications

• Bachelor's Degree in Life Science; PhD preferred.
• 12+ years in biotechnology or pharmaceutical industry.
• 8+ years leading cross-functional project teams in a global matrixed environment; deep drug development knowledge.
• Experience delivering projects on time and within budget with quality.
• Experience orchestrating asset due diligence across scientific/clinical/CMC/Reg/IP/Commercial orgs; comfort with valuation drivers.

Responsibilities

• Provide strategic PM leadership for external innovation activities including due diligence evaluations of external opportunities.
• Lead creation of integrated development plans, timelines, and budgets for due diligence projects.
• Establish tools/templates for the DD process ensuring consistency across evaluations.
• Partner with Search & Evaluation leads to ensure timelines and performance standards are met.
• Facilitate cross-functional meetings; escalate issues to leadership as needed.
• Ensure compliance with confidentiality agreements and governance standards.
• Develop and maintain status reports, dashboards, and decision-support materials for senior leadership.
• Maintain tracking tools to prioritize opportunities and provide leadership with pipeline visibility.
• Engage with internal and external stakeholders to support informed decision-making.
• Drive continuous improvement and adoption of evaluation platforms and AI capabilities.

Skills

Project management

Due diligence

Cross-functional leadership

Stakeholder management

Process improvement

Education

Bachelor's degree in Life Science

PhD preferred

Tools

In Part

AI-enabled search

Job description

Main Responsibilities & Accountabilities

Due Diligence

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Could you be our next Director, Project Management Due Diligence? The job is in our King of Prussia, PA or Waltham MA, office. This is a hybrid position and is onsite three days a week.

Position Description Summary

Provides strategic Project Management leadership for external innovation activities including Due Diligence (DD) evaluations of external opportunities for potential in-licensing or partnership agreements. This role Leads the creation of integrated development plans and associated timelines and budgets for assets under DD evaluation. This role is responsible for establishing tools and templates to be used in the DD process and ensure consistency across all DD to enable consistent and efficient evaluations. This role will partner with the Search & Evaluation leads to ensure cross functional teams are meeting agreed timelines and performance standards. ensuring timely, high-quality execution of evaluations, facilitates cross-functional collaboration, and supports decision-making for portfolio growth and strategic partnerships.

Main Responsibilities & Accountabilities

Due Diligence

• Develop and maintain DD toolkit, templates, documents and knowledge management
• Partner with Search lead and project manage due diligence assessments of potential in-licensing or acquisition opportunities.
• Develop and manage integrated project plans, timelines, budgets and program risks for assets under evaluation.
• Ensure timely completion of scientific, clinical, regulatory, IP, legal, and commercial evaluations.
• Facilitate cross-functional meetings and elevate issues to leadership as needed.

Governance & Reporting

• Ensure compliance with confidentiality agreements and internal governance standards.
• Execute governance processes that enable timely, high-quality decisions on external opportunities, ensuring clear evaluation criteria, defined turnaround times, and strong stakeholder alignment.
• Develop and maintain status reports, dashboards and decision-support materials for senior leadership and governance committees.
• Develop and maintain tracking tools to prioritize external opportunities, monitor deal progress, highlight company inflection points, and provide leadership with transparent pipeline visibility.

Stakeholder Engagement

• Partner with Search lead as key liaison between internal cross-functional teams and external partners, organizing meetings with external companies and orchestrating scientific, clinical, regulatory, and commercial assessments to support informed decision-making.
• Build strong relationships with senior stakeholders across, R&D, Commercial Development, BD, Legal and Finance

Continuous Improvement

• Drive continuous improvement and innovation, enhancing processes and tools—including adoption of evaluation platforms (e.g., In Part) and AI-enabled search capabilities—while coaching team members and fostering collaboration across internal and external stakeholders.
• Drive process optimization for DD and Search workflows.
• Capture lessons learned and implement best practices for future evaluations.
• Mentoring of more junior

Qualifications & Experience Requirements

Bachelor's Degree in Life Science, PHD preferred

12+ years in biotechnology or pharmaceutical industry

8+ years experience as project manager leading cross-functional project teams in a matrixed, global environment, in-depth knowledge in drug research, development and manufacturing processes

Demonstrated experience in delivering projects to meet business objectives on time, within budget and with quality

Experience orchestrating asset due diligence across scientific/clinical/CMC/Reg/IP/Commercial organizations, comfort with valuation drivers and deal critical paths.

Strong understanding of drug development processes and external innovation strategies.

The expected base salary range for this position at hiring is $234,000-260,000 Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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.