Clinical Lead / Clinical Trial Manager - Talent Pipeline Opportunity

Emerald Clinical Trials Inc.; North Carolina; Remote; USD 130,000 - 160,000; Full time

Benefits offered by this job

Competitive Compensation

Hybrid or Remote Work

Career Growth

Global Opportunities

Job summary

Emerald Clinical Trials Inc. is expanding its US presence and seeks experienced Clinical Leads / Clinical Trial Managers for future opportunities. This home-based role oversees global and regional studies with a strong preference for renal, oncology, cardiometabolic, and autoimmune programs.

We value investigators who can drive timelines, patient recruitment, and collaboration with sponsors while assuring FDA/GCP compliance and cross-functional coordination. Travel may be required.

Qualifications

• Bachelor's degree in a scientific or healthcare field is required.
• Strong knowledge of FDA regulations and GCP guidelines.
• Experience leading clinical trials and managing sites/endpoints.

Responsibilities

• Manage operational aspects of clinical trials from initiation through completion.
• Oversee sites and CRA performance.
• Monitor timelines, study metrics, and recruitment performance.
• Lead investigator and sponsor interactions.
• Coordinate study teams and cross-functional activities.
• Support vendor oversight and issue resolution.
• Ensure compliance with FDA requirements, GCP, and SOPs.

Skills

Site management

GCP knowledge

FDA regulations

Stakeholder management

Travel willingness

Education

Bachelor's degree in a scientific or healthcare discipline

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 are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

As part of our strategic growth plans in the United States, Emerald Clinical Trials is building a network of experienced Clinical Leads / Clinical Trial Managers for upcoming opportunities.

Please note: This is a pipelining advertisement. While active hiring needs may vary, we are eager to connect with talented professionals interested in future opportunities as new studies are awarded.

This home-based position offers the opportunity to oversee global and regional clinical studies, with a strong preference for candidates who bring experience within renal, oncology, cardiometabolic & autoimmune diseases.

Your Responsibilities

• Manage operational aspects of clinical trials from initiation through completion.
• Oversee sites and CRA performance.
• Monitor timelines, study metrics, and recruitment performance.
• Lead investigator and sponsor interactions.
• Coordinate study teams and cross-functional activities.
• Support vendor oversight and issue resolution.
• Ensure compliance with FDA requirements, GCP, and company SOPs.
• Contribute to project planning and study execution strategies.

About You

• Bachelor's degree in a scientific or healthcare discipline.
• Prior experience as a Clinical Trial Manager, Clinical Lead or equivalent.
• Strong operational knowledge of site management and monitoring.
• Excellent understanding of FDA regulations and GCP guidelines.
• Ability to manage multiple studies and competing priorities.
• Strong interpersonal and stakeholder-management skills.
• Experience in renal/nephrology clinical trials is highly preferred.
• Willingness to travel when 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.