Tasks
•Lead early-stage discussions with collaborators to define project scope, objectives, timelines, and resource needs
•Draft and refine project documentation, including statements of work (SOWs), project plans, and timelines
•Serve as the primary point of contact between external collaborators and internal R&D, QA, Legal, and Operations teams
•Ensure stakeholder alignment for seamless project execution
•Manage project lifecycle activities, including sample and data transfer coordination, milestone tracking, quality control checkpoints, and risk mitigation
•Ensure deliverables are completed on time and within scope
•Support legal and quality teams with contracting and IP review
•Maintain adherence to internal compliance standards and industry best practices
•Provide regular updates to collaborators and internal leadership
•Lead project meetings, share progress reports, and support final data and report delivery
•Support publication and conference preparation where applicable
Requirements
•Bachelor's or Master's degree in Life Sciences, Oncology, or a related field
•3+ years of experience in project management or operations in a biotech, research, or clinical lab setting
•Strong organizational and interpersonal skills, with a track record of managing complex projects
•Familiarity with scientific collaborations, regulatory environments, and project management tools such as Jira, LIMS, and Benchling
Nice to have
•PhD
•Experience working with multidisciplinary teams across time zones
Conditions
No conditions stated in the posting.
