Clinical Project Manager (United States) - Talent Pipeline Opportunity
Emerald Clinical Trials Randolph County, North Carolina, United States · $160K–$175K/yr
Biotechnology Research · 501-1,000 employees
About the role
Lead the planning, execution, and delivery of clinical studies while managing sponsor relationships and project financial health. Coordinate cross-functional teams and ensure compliance with FDA regulations and ICH-GCP standards.
What they look for
Requirements
Requires a bachelor's degree and at least 7 years of clinical research experience, including 2 years in clinical project management. Candidates should possess strong leadership capabilities and experience in therapeutic areas such as renal, oncology, or cardiometabolic diseases.
Benefits
Full 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
Due to anticipated growth throughout North America, Emerald Clinical Trials is building a talent pipeline of experienced Clinical Project Managers for future clinical development programs.
This is a pipeline posting and may not correspond to an immediate vacancy. We encourage interested candidates to apply so we can engage with talented professionals ahead of future study awards and project launches.
This home-based US position will provide leadership for regional and global clinical trials, with a strong preference for candidates who bring experience within renal, oncology, cardiometabolic & autoimmune diseases.
Your Responsibilities
- Lead the planning, execution, and delivery of clinical studies.
- Manage sponsor relationships and serve as the primary operational contact.
- Oversee timelines, deliverables, budgets, and project financial health.
- Drive study performance and ensure milestones are met.
- Coordinate cross-functional teams across Clinical Operations, Data Management, Medical, Regulatory, and Biostatistics.
- Manage vendors and third-party providers.
- Ensure compliance with FDA regulations, ICH-GCP, and company procedures.
- Conduct risk assessments and implement mitigation plans.
- Support business development initiatives and proposal activities.
About You
- Bachelor's degree required; advanced degree preferred.
- 7+ years of clinical research experience.
- 2+ years of Clinical Project Management experience within a CRO, biotech, or pharmaceutical environment.
- Demonstrated experience managing multi-site or global clinical trials.
- Strong financial, operational, and leadership capabilities.
- Excellent knowledge of GCP and FDA regulations.
- Experience in renal/nephrology clinical trials is highly preferred.
- Ability to travel 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.
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.
The expected salary range for this position is $160,000 - $175,000 per year, depending on experience and qualifications.
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