Director, Project Management Due Diligence

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

Job summary

CSL Behring is seeking an experienced project management leader to drive external innovation activities, including due diligence evaluations for potential in-licensing or partnerships. You will develop integrated development plans, timelines, budgets, and tools to standardize the due diligence process across functions.

The role partners with Search & Evaluation teams to ensure on-time, high-quality assessments and supports decision-making for portfolio growth and strategic alliances.

Qualifications

• Bachelor's Degree in Life Science required; PhD preferred.
• 12+ years in biotechnology or pharmaceutical industry.
• 8+ years leading cross-functional project teams in a global, matrixed environment.
• Demonstrated ability to deliver projects on time, on budget, with quality.
• Experience orchestrating due diligence across scientific, clinical, CMC, regulatory, IP, and commercial domains.

Responsibilities

• Develop and maintain the DD toolkit, templates, and knowledge management.
• Partner with Search lead to manage due diligence assessments of external opportunities.
• Develop and manage integrated project plans, timelines, budgets, and risks.
• Ensure timely completion of scientific, clinical, regulatory, IP, legal, and commercial evaluations.
• Facilitate cross-functional meetings and elevate issues to leadership as needed.

Skills

Due Diligence

Cross-functional leadership

Project management

Drug development

Stakeholder management

Education

Bachelor's Degree in Life Science

PhD preferred

Job description

Main Responsibilities & Accountabilities

Due Diligence

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.