Sydney, New South Wales, Australia · Hybrid
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available. Who We…
Skills: Clinical research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
Sydney, New South Wales, Australia · Hybrid
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available. Who We…
Skills: Clinical research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
Melbourne, Victoria, Australia · Remote OK
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available. Who We…
Skills: Clinical research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
Waitematā, Auckland, New Zealand · Remote OK
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available. Who We…
Skills: Clinical monitoring, Site management, ICH-GCP guidelines, Regulatory compliance, Site selection
Waitematā, Auckland, New Zealand · 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: Clinical trial monitoring, Site management, ICH-GCP guidelines, Regulatory compliance, Site selection
Taipei, Taiwan · Hybrid
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available. Who We…
Skills: Clinical research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
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 research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
Petaling Jaya, Selangor, Malaysia · 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 research, Site management, Monitoring activities, Regulatory compliance, ICH-GCP guidelines
Petaling Jaya, Selangor, Malaysia · 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 guidelines, Regulatory compliance, Site start-up management
Randolph County, North Carolina, United States · Remote OK
$110k–$130k/yr
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 monitoring, Site management, FDA regulations, ICH-GCP, Source data review
Tirana, Central Albania, Albania · 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 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific …
Skills: Clinical monitoring, ICH-GCP, Regulatory compliance, Site management, Source documentation review
Randolph County, North Carolina, United States · Remote Solely
$130k–$160k/yr
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 trial management, Site management, Monitoring, FDA regulations, GCP guidelines
Tirana, Central Albania, Albania · 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 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific …
Skills: Clinical trial management, Clinical operations, Site management, Regulatory compliance, ICH-GCP
Randolph County, North Carolina, United States · Remote OK
$160k–$175k/yr
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, Clinical research, Sponsor relationship management, Budget management, Cross-functional team leadership
Tirana, Central Albania, Albania · 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 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific …
Skills: Clinical project management, Stakeholder engagement, Budget management, ICH-GCP compliance, Risk mitigation
Kwai Tsing District, Hong Kong, China · 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: Clinical trial management, Trial master file maintenance, Site start-up, Regulatory compliance, ICH guidelines
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: Financial planning and analysis, Budgeting, Forecasting, Financial modeling, Variance analysis
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: Financial planning, Financial analysis, Budgeting, Forecasting, Financial modeling
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 financial management, Financial analysis, Revenue recognition, Forecasting, Budgeting
Kuala Selangor, Selangor, Malaysia · 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: Financial planning, Financial analysis, Budgeting, Forecasting, Financial modeling
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The Clinical Research Associate 2 is responsible for site management, monitoring trial activities, and ensuring compliance with regulatory requirements and SOPs. They coordinate site selection, manage trial documentation, and support recruitment efforts to ensure successful trial execution.
Candidates must hold tertiary qualifications in a science or health care discipline and possess over 2 years of experience in on-site monitoring and site management. Proficiency in ICH-GCP guidelines and the ability to travel are mandatory requirements for this role.
Disclaimer: This requisition is currently open for talent pooling purposes. The role is not yet available, but we will review applications and contact suitable candidates as soon as the position becomes available.
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 excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.
With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
Global Expertise. Local Insight. Real Impact.
Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.
Our 1000+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
The Clinical Research Associate 2 is a member of the Clinical Operations group at Emerald Clinical. The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with implementing project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs)
Coordinate the identification, feasibility assessment, and selection of investigators and sites to undertake the trial.
Complete all monitoring activities per the Monitoring Plan along with completing monitoring visit reports, accurately and within the predetermined timeframe.
Prepare, plan, organize, and conduct site evaluation visits and report on these visits to assist in site selection.
Prepare, submit, and/or liaise with regulatory specialist colleagues, regarding the preparation of regulatory packages, importation/exportation requirements, and updates of Ethics Committee packages.
Negotiate site budgets, coordinate for site contract execution, track invoicing, and ensure timely site payments.
Prepare, plan, organize, and conduct site initiation visits.
Develop and maintain appropriate monitoring tools and project-specific documents.
Motivate and train investigators to ensure that the trial site personnel have a good understanding of the protocol, investigational product, and requirements of the trial so they can fulfill their obligations to conduct the trial accurately and to deadlines. Collect, review, and approve essential documents from trial sites, to ensure quality and compliance, and code documents for Trial Master File (TMF) filing.
Reconcile contents of in-house TMF and site’s Investigator Site Files.
Coordinate distribution, tracking, handling, and destruction of investigational product and other trial supplies per site/trial requirements.
Maintain trial information using the clinical trial management system and any other tracking and reporting tools for the trial.
Support strategies to boost recruitment efforts.
Tertiary qualifications in a related science or health care discipline.
Previous experience in clinical trials within an academic, CRO, or pharmaceutical environment with more than 2 years' experience in on-site monitoring and site management experience is mandatory
Experience in Renal and/or Oncology clinical trials is a plus.
Demonstrate practical knowledge of ICH-GCP guidelines and global and local ethical and regulatory research requirements.
Display competence in the following technical areas: ethical and participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts and clinical research design, and issue escalation management.
Demonstrate competence in the following business skill areas: negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking.
Demonstrate solid interpersonal communication, presentation skills, and flexibility to work well within a multi-disciplinary team both autonomously and with a wide range of varying stakeholders
Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.
Ability and willingness to travel
Why Join Us?
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:
We understand that great work happens when people feel valued and supported. That’s why we provide:
Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.
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
