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 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
800+ employees that span across Asia-Pacific, Europe, and the Americas
areembedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. About the Role We are looking for an experienced
Site Contracts Lead
to join our dynamic Project Management team. This role is key to ensuring the success of our clinical trials by driving all budget and contract-related activities with both academic and commercial clients. You’ll work cross-functionally to oversee contract development, site negotiations, and budget management. You will also partner closely with sponsors, vendors, and clinical operations staff.
This is a hands-on, impactful role ideal for someone with strong contract negotiation experience, a strategic mindset, and a collaborative approach to problem-solving. Your Responsibilities Lead contract and budget development across multiple studies
Serve as the main point of contact for sites regarding all contract and budget matters
Oversee site contract negotiations and ensure alignment with sponsor expectations
Partner with clinical operations and project teams to manage timelines, deliverables, and change requests
Coordinate project-specific vendor activities and site payment processes
Track and forecast project budgets, scope changes, and key milestones
Contribute to internal process improvements and support training activities
Ensure compliance with ICH-GCP, SOPs, and all relevant regulatory guidelines
About You To be successful in this role, you will have: Qualified lawyer is preferred
Prior experience in a CRO, pharma, or academic setting supporting clinical trials
Strong background in site contract and budget negotiation
Excellent interpersonal and communication skills, with experience managing virtual teams
Good understanding of ICH-GCP and clinical research regulations
Proficient in Microsoft Office and clinical trial management tools
Self-motivated, detail-oriented, and adaptable to fast-paced environments
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: •
Purpose-Driven Work : You’ll 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. What We Offer 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 to reflect your skills and experience. •
Flexibility : Enjoy hybrid or remote working arrangements, depending on your location and role. •
Career Growth : Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role. •
Employee Wellbeing : Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events. •
Global Opportunities : Be part of a company with international reach, offering you exposure to diverse projects and clients.
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.
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