Manager, Clinical Supply

Who is BlueRock?

BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investigational cell therapies, bemdaneprocel (BRT-DA01) for the treatment of Parkinson’s disease and OpCT-001 for the treatment of primary photoreceptor diseases are clinical stage programs. BlueRock was founded in 2016 as a joint venture of Versant Ventures and Leaps by Bayer. Our culture is defined by the courage to persist regardless of the challenge, the urgency to transform medicine and deliver hope, integrity guided by mission, and community-mindedness with the understanding that we are all part of something bigger than ourselves.

What Are We Doing?

Our foundational science harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit.
We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options.
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives.

The Manager, Clinical Supply is responsible for leading cross-functional clinical supply planning to ensure alignment between patient demand, surgical schedules, manufacturing network capacity, and supply readiness. This role serves as a key planning interface across Clinical Operations, Supply Chain, Manufacturing, and external partners, translating evolving clinical demand signals into actionable operational plans for late-stage clinical programs. The position drives integrated planning forums, scenario analysis, risk management, and leadership reporting to enable reliable, scalable, and compliant trial execution.

Responsibilities::
• Own CSI hub scheduling and forecast alignment based on trial enrollment and treatment center surgical capacity

• Lead the monthly rolling forecast process with Clinical Operations, including demand/supply reconciliation, assumptions, constraints, and action planning

• Partner with Clinical Ops to translate enrollment updates, protocol changes, and planning scenarios into hub plans and supply readiness actions

• Serve as PM and lead facilitator for the Clinical Supply Integrated Planning (CSIP) forum, including agenda setting, pre-reads, decision capture, action tracking, and risk escalation

• Lead cross-functional planning standups across Supply Chain to ensure readiness, alignment on constraints, and clear inter-functional commitments

• Represent Tech Ops / Clinical Supply as the primary planning interface in Clinical Operations meetings and program forums

• Build, maintain, and improve integrated planning dashboards, KPIs, and leadership reporting

• Lead scenario planning and tradeoff analysis, and provide recommendations to support leadership decision-making

• Consolidate clinical and non-clinical CSI hub demand, including engineering runs, tech transfer, and training activities, into one integrated planning view

• Standardize and continuously improve integrated planning processes, governance, and documentation, while supporting scalable operating models and providing backup coverage for critical logistics operations as needed

Minimum Requirements::
• Bachelor’s degree in Supply Chain, Engineering, Life Sciences, Business, or related field

• Manager: 11+ years of experience in clinical supply, manufacturing operations, supply chain planning, integrated planning, or program management within biopharma/pharma

• Demonstrated experience translating clinical demand signals into operational plans across manufacturing networks (internal and/or external/CDMO)

• Strong program management skills (governance, stakeholder alignment, action/risk management, executive communication)

• Strong analytical capability: KPI definition, dashboarding, and data storytelling for decision-making

• Experience operating in regulated environments and familiarity with GxP expectations and documentation discipline

• Proficiency with planning and reporting tools (e.g., Excel, Smartsheet) preferred; ERP familiarity such as SAP/Oracle a plus)

• Excellent communication and facilitation skills; ability to lead without authority and drive alignment across competing priorities

• Compare clinical trial portfolios and apply phase appropriate planning standards and proactively surface conflict, tradeoffs and recommendations

• This role is a hybrid role based out of Toronto

Base Salary Range: $130,000 - $155,000

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BlueRock Therapeutics Company Culture Highlights
Winner of Boston Business Journal's Best Places to Work (Mid-size Company) 2023
Winner of Comparably's Award for Best Company for Diversity 2022
Winner of Comparably's Award for Best Company for Women 2022
Winner of Comparably's Award for Best CEO 2022
BlueRock Therapeutics is ranked in the top 5% of companies for Overall Culture on Comparably.
Engineering Department is ranked in the top 5% of companies for Overall Culture on Comparably.

Check us out on Comparably: https://www.comparably.com/companies/bluerock-therapeutics
Follow us on Linkedin: https://www.linkedin.com/company/bluerocktx/

Equal Opportunity Workplace: At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace. Please let us know if you require disability-related accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs.