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Hemab is a clinical-stage biotech company focused on addressing the high unmet needs of patients with rare bleeding and thrombotic disorders. The Vendor and Project Manager serves as the primary operational point of contact for ongoing work at Hemab’s NCD, Bioanalytical, and DMPK/Clinical Pharmacology vendors. Reporting to Heads of QCP and NCD, this individual will manage the full vendor lifecycle—from contracting and onboarding through performance oversight—ensuring that external partnerships operate efficiently, on time, and within budget across Hemab’s portfolio.
Job Responsibility:
Serve as the primary operational point of contact (non-scientific) for on-going work at our NCD, Bioanalytical, and DMPK/ Clinical Pharmacology vendors with guidance from corresponding functional area leads
Responsible for vendor management including overseeing financial and legal (contracting/ billing/ invoicing), operational (managing sample/materials shipments), and project management (timelines, resourcing) aspects of ongoing work
Develop & maintain project trackers and utilize project management tools to keep stakeholders informed while providing transparent communication on project status
Lead vendors relationships as if they are an extension of Hemab
Build and maintain strong relationships with vendors to grow lasting and highly agile collaborations
Monitor vendor performance, including tracking Key Performance Indicators (KPIs) and conduct Quarterly Business Reviews as needed to always ensure efficient and effective collaboration
Assist QCP and NCD functional area leads in vendor evaluation, selection and onboarding
Assist functional area leads and quality assurance teams in coordinating quality audits of vendors adhering to GxP compliance
Collaborate with Clinical Operations team to track/manage sample shipments and provide input on Lab Manuals as needed with regards to sample shipping procedures
Be pro-active in identifying risks and proposing resolution/ mitigation strategies with vendors including adhering to contracting agreements and good governance policies
Requirements:
Minimum BS, preferably MS in a life science or related field
4+ years of experience in a project management or operations role within drug development, preferably with exposure to DMPK, bioanalytical, or nonclinical functions
Proficient in project management software
experience with Microsoft Project, Coda, and/or other project management platforms is required
Demonstrated experience developing and tracking KPIs across the vendor lifecycle
Meticulous attention to detail and excellent written and verbal communication skills, with demonstrated ability to keep cross-functional stakeholders informed and aligned
Demonstrated experience negotiating and managing contracts with CROs and vendors, including oversight of financial and legal aspects of vendor engagements
Nice to have:
Prior experience in early-stage biotech companies with lean teams and evolving priorities
Knowledge of GxPs and application to operational oversight of nonclinical and clinical studies
Collaboration with Quality Assurance to perform vendor audits or engaged in internal/external audit processes
Collaboration with Clinical Operations on sample tracking and related tasks