Tirana, Central Albania, Albania · Remote OK
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise…
Skills: Project Management Office, Data Analysis, KPI Development, Stakeholder Engagement, Project Governance
Randolph County, North Carolina, United States · Remote Solely
$155k–$175k/yr
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise…
Skills: Clinical Project Management, Nephrology, Budget Management, ICH-GCP, Vendor Management
Randolph County, North Carolina, United States · Remote OK
$100k–$117k/yr
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise…
Skills: Onboarding, Employee Relations, Compliance & Risk Management, Compensation & Benefits, Performance & Talent Management
Warsaw, Masovian Voivodeship, Poland · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Site Management, Clinical Monitoring, ICH-GCP Guidelines, Regulatory Compliance, Site Selection
Warsaw, Masovian Voivodeship, Poland · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Site Management, Clinical Monitoring, ICH-GCP Guidelines, Regulatory Compliance, Site Selection
Sydney, New South Wales, Australia · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Early Phase Strategy, Clinical Trial Design, RFP Assessment, Bid Defence, Operational Risk Assessment
Seoul, South Korea · Hybrid
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Clinical Trial Monitoring, Site Management, ICH/GCP Compliance, Regulatory Submission, Budget Negotiation
Tirana, Central Albania, Albania · Remote Solely
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise…
Skills: Project Management, Nephrology, Clinical Trial Execution, Financial Oversight, Budget Management
Beijing, Beijing, China · Hybrid
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Project Management, Clinical Trial Management, Renal/Nephrology Expertise, ICH GCP, Budget Management
Beijing, Beijing, China · Hybrid
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Project Management, Clinical Trial Management, ICH GCP, Renal Research, Budget Management
Taipei, Taiwan · Hybrid
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Clinical Development Strategy, Medical Monitoring, GCP Compliance, Pharmacovigilance, Project Management
Taipei, Taiwan · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Medical Monitoring, Clinical Trial Oversight, GCP Compliance, Safety Assessment, Protocol Development
Taipei, Taiwan · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Medical Monitoring, Clinical Trial Oversight, GCP, Medical Review, Safety Assessment
Seoul, South Korea · On-site
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Trial Master File (TMF) Management, Clinical Trial Start-up, ICH/GCP Guidelines, Regulatory Compliance, Quality Control
Sydney, New South Wales, Australia · Remote OK
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific e…
Skills: Project Management, Clinical Trial Management, ICH GCP, Financial Management, Client Management
Tirana, Central Albania, Albania · Remote Solely
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific …
Skills: Clinical Project Management, Renal Research, Financial Oversight, ICH-GCP Compliance, Vendor Management
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The PMO Analyst will drive consistency and operational efficiency by maintaining project standards and developing performance dashboards. They will collaborate with Project Managers to ensure adherence to SOPs and regulatory requirements while providing actionable insights to senior leadership.
Candidates should hold a Bachelor's degree in Life Sciences, Business, or Project Management with 2-4 years of experience in a PMO or analytical role. Proficiency in project management and data analysis tools like MS Project and Power BI is required, preferably within a CRO or pharmaceutical environment.
At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.
Our therapeutic expertise spans renal, cardiometabolic, and oncology - areas where we make a significant impact on improving global health.
At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results - bringing therapies to patients in need.
We are seeking a detail-oriented and analytical PMO Analyst to support our Project Management Office in driving consistency, governance, and operational efficiency across clinical and business projects.
In this role, you will play a key part in strengthening project oversight by maintaining standards, developing meaningful reporting insights, and ensuring adherence to best practices and regulatory requirements. You will work closely with Project Managers and cross-functional stakeholders to enhance visibility, improve decision-making, and support continuous improvement across the organisation.
This is an excellent opportunity for someone who thrives on data, enjoys problem-solving, and is passionate about improving project delivery in a clinical research environment.
Support the implementation and ongoing maintenance of PMO standards, methodologies, and tools across clinical and operational projects
Develop and maintain project dashboards, KPIs, and performance metrics to provide actionable insights
Assist study teams with project timeline tracking and updates
Prepare status reports, presentations, and governance materials for senior leadership and stakeholders
Facilitate project governance processes, including stage gates, audits, and reporting cycles
Collaborate with Project Managers to improve adherence to SOPs, regulatory requirements, and best practices
Analyse project data to identify trends, risks, and opportunities for improvement
Support change management initiatives and continuous improvement efforts across the PMO
Assist in preparing and facilitating Project Management Forum meetings
Contribute to the development and enhancement of tools and processes to support high-quality project documentation
Support project resourcing activities, including coordination for holiday cover
To be successful in this role, you will have:
Bachelor’s degree in Life Sciences, Business Administration, Project Management, or a related field
2–4 years of experience in a PMO, project coordination, or analytical role, ideally within a CRO or pharmaceutical organisation
Understanding of clinical trial processes and GCP/regulatory frameworks (preferred)
Proficiency in project management tools (e.g., MS Project, Smartsheet) and data analysis tools (e.g., Excel, Power BI)
Strong organisational, analytical, and problem-solving skills
Excellent communication and stakeholder engagement abilities
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first - both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here’s what makes us stand out:
Purpose-Driven Work: Contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
We understand that great work happens when people feel valued and supported. That’s why we provide:
Competitive Compensation: A tailored salary and benefits package reflecting your experience and expertise
Flexibility: Hybrid or remote working options depending on your location
Career Growth: Access to global development opportunities and exposure to leading scientific experts
Employee Wellbeing: Programs designed to support work-life balance, recognition, and team connection
Global Opportunities: Work on international studies with diverse clients and teams
We are an equal-opportunity employer and encourage applications from all qualified candidates.
Emerald Clinical is a global, full-service CRO with over 25 years of experience delivering end-to-end clinical trial solutions. Headquartered in Singapore, we support Phase I–IV and real-world studies across all therapy areas through a team of 800+ professionals working in 40+ countries, backed by a collaborative network spanning 70+ locations worldwide. We partner with more than 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms, providing scientific excellence and operational expertise to advance innovative therapies. Our core specialties include Renal, Oncology, Autoimmune, Ophthalmology, Cardiometabolic, and Early Phase development.
Offices: #32-01, 300 Beach Road, The Concourse, Singapore, Singapore 199555, SG
Emerald Clinical is a global, full-service CRO with over 25 years of experience delivering end-to-end clinical trial solutions. Headquartered in Singapore, we support Phase I–IV and real-world studies across all therapy areas through a team of 800+ professionals working in 40+ countries, backed by a collaborative network spanning 70+ locations worldwide. We partner with more than 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms, providing scientific excellence and operational expertise to advance innovative therapies. Our core specialties include Renal, Oncology, Autoimmune, Ophthalmology, Cardiometabolic, and Early Phase development.
Offices: #32-01, 300 Beach Road, The Concourse, Singapore, Singapore 199555, SG
