About The Position

We are seeking a proactive and detail-oriented Project Manager to support the delivery of pathology-focused clinical trial projects at Diagnexia Analytix. Sitting under the Clinical Trial Manager, this role will act as the operational driver of projects — ensuring that timelines, deliverables, and quality standards are met across complex, multi-stakeholder clinical studies. The Project Manager will not design the science, but will make sure the science happens: coordinating vendors, labs, pathologists, and internal teams, while keeping communication clear and projects audit-ready.

Requirements

  • Degree in life sciences, biomedical sciences, or a related discipline.
  • 3–5 years’ experience in clinical trial project management, CRO operations, or translational/biomarker projects.
  • Strong knowledge of GCP/GCLP and ICH E6 standards.
  • Proven ability to deliver multi-stakeholder projects on time and within scope.
  • Excellent organizational skills; able to manage multiple vendors, labs, and deliverables.
  • Strong communication skills, with experience preparing reports, dashboards, and running status calls.
  • Ability to anticipate issues, escalate appropriately, and drive solutions.
  • Proficiency with project management tools (e.g., Smartsheet, MS Project, Asana) and shared document platforms.

Nice To Haves

  • Exposure to pathology, histology, or biomarker assay workflows.
  • Experience coordinating pathologists and pathology vendors.
  • Familiarity with digital pathology platforms (WSI, image hosting, secure data transfer).
  • Therapeutic area experience in oncology, immunology, or liver disease trials.
  • Formal PM certification (PMP, PRINCE2) or Lean/Agile training.
  • Strong interpersonal skills: able to “manage up” to senior stakeholders while motivating delivery teams.
  • Experience in a scale-up/fast-growing environment.

Responsibilities

  • Translate Statements of Work (SoWs) into actionable project plans, timelines, and trackers.
  • Manage day-to-day execution, logistics, and operational workflows.
  • Oversee sample flow, staining, scanning, and digital pathology processes.
  • Pathologist Management, training and communication
  • Serve as a central point of contact between sponsor, CRO, central labs, and internal teams.
  • Organize and document sponsor calls, training sessions, consensus/adjudication meetings.
  • Maintain action logs, decision records, and issue escalation pathways.
  • Ensure all activities follow GCP/GCLP, ICH E6, and regulatory standards.
  • Support preparation of validation reports, pathology manuals, final study reports, and archival outputs.
  • Track QC metrics, deviations, CAPA actions, and maintain audit readiness.
  • Maintain a risk register for timelines, logistics, and deliverables.
  • Coordinate structured change control processes when scope or timelines shift.

Benefits

  • 💰 Competitive salary with annual performance-based increases. Rewarding your impact and growth
  • 🩺 Healthcare benefits, giving you peace of mind to focus on what you do best
  • 🌴 Annual leave with service increments - Means more time to recharge and enjoy life outside work
  • 💡 Pension contributions, helping you build a secure future
  • 🚀 Work with a world-class, high-performing team in a hyper-growth startup. You’ll earn fast, make an impact, and shape the future
  • 📈 Regular feedback and clear career growth opportunities. You keep developing and moving forward
  • 🌍 A collaborative, supportive, multicultural team. Here you’ll feel valued and inspired every day
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service