SAB BIO · 3 months ago
Project Management Associate, Vendors & Contracts
SAB BIO is a precommercial biotech company focused on drug development, and they are seeking a Project Management Associate to support strategic and cross-functional projects. The role involves collaborating with scientific, clinical, regulatory, and commercial teams, managing project plans, tracking progress, and ensuring alignment with company objectives.
BiotechnologyClinical TrialsTherapeutics
Responsibilities
Support Director of Program Management in coordinating internal and external team efforts, ensuring alignment of project timelines, deliverables, and resources
Act as a liaison between various departments (R&D, Clinical, Regulatory Affairs, Quality, Business Development, and Affiliates) to facilitate communication and information flow
Assist in developing detailed project plans, timelines, and budgets, and track progress against milestones. Ensure risks are identified, mitigated, and communicated
Support vendor interaction and oversight, including CROs, CDMOs, and other service providers, ensuring deliverables are met within scope, budget, and timeline
Assist in contract review, routing, tracking, and execution, ensuring alignment across legal, finance, and operational teams. Support business development and affiliate-related agreements
Utilize and maintain contract management software (e.g., LinkSquares) and electronic signature tools (Part 11–compliant DocuSign) to ensure compliance, traceability, and timely execution of agreements
Prepare and maintain project documentation, including meeting minutes, project reports, and status updates. Assist in the preparation of presentations for senior leadership and stakeholders
Coordinate and manage project-related meetings, including internal team meetings and external vendor or collaborator meetings. Help manage action items and follow-up to ensure timely delivery
Monitor project risks, raise concerns as appropriate, and support the development of mitigation strategies
Assist in analyzing data from ongoing projects and helping to prepare reports for key decision-making processes
Help ensure that all project activities comply with regulatory standards, company policies, and industry best practices
Other duties/responsibilities as assigned
Qualification
Required
A Bachelor's degree is required
1-3 years of experience in biotech, pharmaceutical, or healthcare-related industries
Prior experience in project management or project coordination or contract/vendor support is highly preferred
Familiarity with biotech industry regulations, drug development stages, and clinical trials
Proficiency in MS Office (Excel, Word, PowerPoint), project management tools (e.g., MS Project, Smart Sheet, Asana, or similar)
Experience with contract management and electronic signature tools
Exceptionally strong organizational and project management skills and demonstrated ability to deliver accurate work product in a timely manner
Ability to work in a fast-paced, cross-functional team environment with the ability to prioritize and manage multiple tasks simultaneously
Team player with a collaborative mindset
Ability to handle ambiguity and manage changing priorities in a dynamic environment
Excellent written and verbal communication skills
Strong problem-solving and analytical abilities
Preferred
A focus in Life Sciences, Chemistry, Biochemistry or related science degree is preferred
A Master's degree and/or PMP certification is a plus
Experience in preclinical, clinical, or regulatory development is a plus
Company
SAB BIO
A clinical-stage biopharmaceutical company with a novel immunotherapy platform that is developing fully-human anti-thymocyte immunoglobulin (hIgG) for delaying the onset or progression of type 1 diabetes (T1D)
Funding
Current Stage
Public CompanyTotal Funding
$361.32MKey Investors
RA Capital ManagementU.S. Department of DefenseSouth Dakota Equity Partners
2025-07-21Post Ipo Equity· $175M
2023-10-02Post Ipo Equity· $130M
2023-01-18Grant· $8M
Recent News
2026-01-08
2026-01-07
2026-01-06
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