Clinical Lead / Clinical Trial Manager

Emerald Clinical Trials; Clayton (NC); Remote; USD 130,000 - 160,000; Full time

Job summary

Emerald Clinical Trials is seeking an experienced Clinical Lead to join our U.S. team. This home‑based role leads global and regional trials across multiple therapeutic areas, with a strong focus on renal research. The ideal candidate has trial management and leadership experience, plus solid GCP and FDA regulatory knowledge.

You will mentor CRAs and site staff, manage timelines and budgets, collaborate with sponsors and investigators, and travel up to 20% as required.

Qualifications

• Renal experience and clinical trial leadership are required.
• Strong knowledge of GCP and FDA regulations.
• Ability to manage multiple trials, timelines, and stakeholders.

Responsibilities

• Oversee clinical trials from start-up to close-out.
• Lead site selection and feasibility assessments with CRAs and investigators.
• Manage study timelines, budgets, and deliverables, ensuring protocol adherence and data integrity.
• Collaborate with sponsors, investigators, and project teams.
• Ensure compliance with GCP, FDA regulations, and SOPs.
• Train and mentor CRAs and site staff.

Skills

Renal experience

Clinical trial leadership

GCP knowledge

FDA regulations

Multi‑project management

Strong communication

Education

Bachelor’s degree in science (RN preferred)

CCRA or CCRP certification

Job description

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 seeking an experienced Clinical Lead to join our growing team in the United States. This is a home-based role, offering flexibility while providing the opportunity to lead global and regional clinical trials across multiple therapeutic areas. The ideal candidate will have experience managing clinical trials and a strong background in project leadership, clinical operations, and strategic trial execution.

Your Responsibilities

• Oversee clinical trials, ensuring successful execution from start-up to close-out.
• Lead site selection and feasibility assessments, working closely with CRAs and investigators.
• Manage study timelines, budgets, and deliverables, ensuring adherence to project objectives.
• Provide oversight on protocol administration, site initiation, monitoring, and study progress.
• Collaborate cross-functionally with internal and external stakeholders, including sponsors, investigators, and project teams.
• Ensure compliance with GCP, FDA regulations, and company SOPs.
• Train and mentor CRAs and site staff, ensuring protocol adherence and data integrity.

About You

To be successful in this role, you will have:

• Renal experience
• Bachelor’s degree in a science-related field (RN preferred) with industry experience, including 1-2 years as a Clinical Trial Manager/Clinical Lead.
• Strong background in monitoring and site management, preferably with experience in oncology or other complex indications.
• CCRA or CCRP certification is strongly preferred.
• Excellent knowledge of GCP, FDA regulations, and clinical trial best practices.
• Ability to manage multiple projects, timelines, and stakeholders efficiently.
• Strong leadership, problem‑solving, and communication skills.
• Willingness to travel up to 20% as required.

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.

We are an equal‑opportunity employer and encourage applications from all qualified candidates.

The expected salary range for this position is $130,000 - $160,000 per year, depending on experience and qualifications.