$90K - 120K a year
Manage and coordinate clinical trial project delivery, stakeholder communication, quality compliance, and risk/change management for pathology-focused studies.
Requires 3-5 years clinical trial project management experience, knowledge of GCP/GCLP and ICH E6 standards, strong organizational and communication skills, and proficiency with project management tools.
Role Type and Location • Work from home role - this role requires you to be based full time in the East Coast, USA. Eligibility to work • Unfortunately, we cannot offer USA based Visa sponsorship for this full time USA BASED role. Role Summary 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. Key Responsibilities Project Delivery & Coordination • 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 Stakeholder 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. Quality & Compliance • 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. Risk & Change Management • Maintain a risk register for timelines, logistics, and deliverables. • Coordinate structured change control processes when scope or timelines shift. Required Skills & Experience (Must-Have) • 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. Preferred Skills & Experience (Nice-to-Have) • 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. Ideal Candidate Profile A “doer” who thrives on making things happen in complex clinical projects. Comfortable working alongside scientific leaders while taking responsibility for operations, timelines, and compliance. Highly organized, proactive, and able to bring structure and accountability to dynamic, multi-stakeholder studies. What are the benefits of working with Deciphex 💰 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 About the Company Through the work that we do, the team at Deciphex helps pharma to accelerate the process of essential drug development and helps patients to get timely and accurate diagnosis. Founded in Dublin in 2017, Deciphex has scaled rapidly to a team of over 180 people and counting who are providing software solutions to address the pathology gap in research pathology and clinical areas. We have offices in Dublin, Exeter, Oxford, Toronto and Chicago and are expanding our team throughout the world. We are software developers, clinical specialists, AI engineers, operations professionals and so much more, all working as one team to support our customers and patients. Our team culture is built on trust. We give our team the space they need to deliver results and the environment to ensure they can enjoy doing it. We are looking for highly motivated individuals who are excited to take on challenges and value making a difference in their day-to-day work. This is a unique opportunity to make a difference in the emerging Digital Pathology field. Read more about Deciphex here and more about our incredible team on our Careers Page here
This job posting was last updated on 10/15/2025