* Salary estimates based on industry data for similar roles
Launch Your Clinical Research Career at a Global CRO with Local Impact
Emerald Clinical Trials, a global Contract Research Organization (CRO) with deep roots in the Asia-Pacific region, is seeking a dedicated Clinical Trial Specialist to join our Clinical Operations team. This is a foundational role perfect for a detail-oriented professional looking to build a career in clinical research. You will be at the heart of our trial execution, responsible for the critical start-up phase and the integrity of the Trial Master File (TMF), ensuring we can efficiently bring new therapies to patients in need across renal, cardiometabolic, and oncology fields.
Key Responsibilities & Impact:
- Site Start-Up & Feasibility: Act as a key point of contact for clinical trial sites during the start-up phase. You will assist with feasibility assessments, guide sites in collecting essential document packets (EDPs), and manage submissions to IRBs/Ethics Committees to accelerate trial initiation.
- Trial Master File (TMF) Excellence: Take ownership of the TMF setup, maintenance, and quality control (QC) in both electronic and hard-copy systems. Your meticulous work will ensure inspection-ready compliance throughout the trial lifecycle and support seamless study archiving.
- Process Coordination & Quality Control: Perform quality checks on documents and communications, support data entry in Clinical Trial Management Systems (CTMS), and assist with tracking investigator payments. Your focus on quality ensures accuracy and efficiency across all trial activities.
- Collaborative Project Support: Work closely with Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs), and Project Managers as an integral in-house specialist, providing the essential documentation and administrative support that keeps global trials on track.
About You: The Ideal Candidate
- You hold a college/university degree or have 1+ years of relevant experience in a clinical, administrative, or life sciences setting.
- You are a quick learner with a keen eye for detail and a passion for processes and organization.
- You thrive in a supportive, team-based environment and are eager to develop expertise in ICH/GCP guidelines and regulatory requirements.
- Familiarity with medical terminology or clinical research processes is a strong advantage, but a willingness to learn is most important.
Why Build Your Career at Emerald Clinical Trials?
At Emerald, we believe our success is driven by our people. We combine global resources with local expertise in the APAC region to deliver meaningful clinical research. When you join our team, you're not just filling a role—you're contributing to a purpose-driven mission to improve global health.
What We Offer You:
- A Clear Career Pathway: This role is designed for growth. We provide structured training and mentorship to help you develop from a specialist into potential future roles in Clinical Monitoring, Data Management, or Project Management.
- Meaningful Work: Contribute to clinical trials in critical therapeutic areas like renal, cardiometabolic, and oncology, where your work directly impacts patient lives.
- Global & Collaborative Culture: Be part of an international team that values diverse perspectives, knowledge sharing, and innovative problem-solving.
- Comprehensive Support: We invest in your well-being and professional development with competitive compensation, health benefits, and team-building initiatives that foster a connected community.
Ready to make a difference in global health? If you are an organized, proactive individual ready to launch your career in clinical research, we encourage you to apply.
Emerald Clinical Trials is an equal-opportunity employer committed to creating a diverse and inclusive workplace.
