Project Coordinator Job at ClinLab Solutions Group, Cambridge, MA

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  • ClinLab Solutions Group
  • Cambridge, MA

Job Description

Overview:

This role supports a variety of outsourced preclinical studies by coordinating timelines, data flow, and communication between internal teams and external partners. The position is highly cross-functional and requires strong organization, attention to detail, and comfort managing multiple parallel workflows. This is an onsite position.

Key Responsibilities

  • Act as the central point of contact for planning and organizing outsourced preclinical studies.
  • Track study requests, deliverables, decisions, and milestones using project management tools (e.g., Smartsheet or similar).
  • Prepare and distribute meeting notes, summaries, and action items following internal and external study-related discussions.
  • Maintain visibility into study progress by developing dashboards, metrics, Gantt charts, and other project tracking tools.
  • Gather feedback from internal scientists, external vendors/CROs, and functional leads to ensure alignment on expectations and timelines.
  • Identify potential bottlenecks or risks in ongoing studies and escalate issues as needed.
  • Support coordination across research, operations, quality, regulatory, and vendor partners to ensure study requirements are met.
  • Provide consistent status updates to project stakeholders and leadership.

Qualifications

  • Bachelor’s degree in a life science, biotechnology, or project-management–related field.
  • Experience supporting projects in biotech, pharma, or research environments.
  • Experience working with project-tracking platforms and creating dashboards, timelines, and reports.
  • Strong communication skills, including the ability to write clear meeting minutes and synthesize technical information.
  • Excellent organizational skills with the ability to manage multiple concurrent studies and deadlines.
  • Familiarity with cross-functional collaboration and coordinating with external vendors or CROs.
  • Exposure to preclinical or non-clinical study workflows (e.g., IND-enabling studies) is a plus.
  • Ability to operate in fast-moving, ambiguous environments and help drive alignment across teams.

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