Senior Clinical Delivery Leader

Emerald Clinical; United States; Remote; USD 145,000 - 165,000; Full time

Job summary

Emerald Clinical is seeking a Senior Clinical Delivery Leader in the USA for a home-based role. This position involves managing global clinical trials across therapeutic areas, requiring strong leadership and extensive clinical trial management experience. The role offers competitive compensation, flexibility, and opportunities for career growth within a purpose-driven organization.

Benefits

Competitive Compensation

Flexibility

Career Growth

Employee Wellbeing

Global Opportunities

Qualifications

• 7+ years of industry experience, including 2-3 years as a Clinical Trial Manager.
• Nephrology or Oncology experience is mandatory.

Responsibilities

• Oversee clinical trials from start-up to close-out.
• Lead site selection and feasibility assessments.
• Ensure compliance with GCP and FDA regulations.

Skills

Leadership

Problem-Solving

Communication

Education

Bachelor’s degree in a science-related field

Tools

GCP

FDA regulations

Job description

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At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

About the Role

We are seeking an experienced Senior Clinical Delivery Leader to join our growing team in the USA. 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

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

About You

To be successful in this role, you will have:

• Nephrology (renal trials) or Oncology experience is mandatory.
• Bachelor’s degree in a science-related field (RN preferred) with 7+ years of industry experience, including 2-3 years as a Clinical Trial Manager or Clinical Trial 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.

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 $145,000 - $165,000 per year, depending on experience and qualifications.