Sr Clinical Trial Manager

Verona Pharma; Raleigh (NC); Hybrid; USD 100,000 - 180,000; Full time

Job summary

A leading company in respiratory drug development, Verona Pharma, is seeking a Sr Clinical Trial Manager to oversee global clinical trials focused on COPD and other respiratory indications. The ideal candidate will drive clinical study execution and collaborate across teams to maintain high-quality standards in research. This role offers a chance to make a significant impact on patient care and treatment outcomes.

Benefits

Remote work flexibility

Collaborative and inclusive culture

Qualifications

• 8+ years of global clinical trial management experience in Pharma or Biotech, specifically in Phase 2/3 respiratory trials.
• Proficient with clinical trial platforms and strong understanding of regulatory requirements.
• Must be located in the Triangle area with hybrid work ability.

Responsibilities

• Manage end-to-end operational management of global Phase 2/3 clinical trials.
• Coordinate with CROs, manage budgets and timelines, ensure safety and compliance.
• Lead study meetings and provide training for stakeholders.

Skills

Leadership

Project Management

Communication

Problem Solving

Knowledge of GCP and ICH guidelines

Education

Bachelor’s degree (MS/PhD preferred)

Tools

Clinical trial platforms (e.g., eTMF, eDC)

MS Office and Excel

Job description

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Join to apply for the Sr Clinical Trial Manager role at Verona Pharma

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At Verona Pharma, we are passionate about transforming the lives of millions of people living with chronic respiratory diseases. With our first product now approved by the US FDA, we’re just getting started. Our innovative respiratory pipeline targets a range of conditions, including non-CF bronchiectasis, cystic fibrosis (CF), and asthma, driven by a commitment to bringing relief to patients navigating the challenges of progressive respiratory conditions.

Joining Verona means being part of a forward-thinking team that’s redefining what’s possible in drug development and commercialization. Guided by experienced leadership, we embrace a collaborative, diverse, and inclusive culture where your contributions can help shape a healthier future for patients worldwide. Be part of a mission-driven organization where your work has a direct impact on improving quality of life.

We’re hiring a Sr Clinical Trial Manager who will be responsible for the end-to-end operational management of global Phase 2/3 clinical trials, with a strong focus on respiratory indications, especially COPD. This role reports to the Executive Director, Clinical Development and will lead all aspects of clinical study execution - protocol development, vendor/CRO oversight, site management, data integrity, safety, budget, timelines, and regulatory compliance.

What You’ll Do:

• Lead and manage all operational components of global clinical trials.
• Oversee study timelines, budgets, and milestones.
• Coordinate with cross-functional teams, CROs, and vendors to ensure high-quality study execution.
• Manage site activation, monitoring, data review, and protocol compliance.
• Conduct risk assessments, ensure inspection readiness, and manage safety and pharmacovigilance processes.
• Lead study meetings and provide training to internal and external stakeholders.
• Support study document development and clinical study reporting.
• Other duties as assigned.

What You’ll Bring:

• Bachelor’s degree required (MS/PhD preferred).
• 8+ years of global clinical trial management experience in Pharma or Biotech, specifically in Phase 2/3 respiratory trials.
• Proven leadership experience and ability to manage vendors, budgets, and cross-functional teams.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Expertise in respiratory therapeutic areas, especially COPD.
• Excellent communication, problem-solving, and project management skills.
• Proficiency with clinical trial platforms (e.g., eTMF, eDC), MS Office and Excel.
• Must be based in the Triangle (Raleigh/Durham/Chapel Hill area) with the ability to work in a hybrid capacity (in-office as needed for meetings and collaboration).

Why Join Verona?

At Verona, you'll have the chance to be part of a team bringing first-in-class treatments to patients who need them most. We offer:

• A collaborative and inclusive culture that values your contributions.
• Remote work flexibility for a better work-life balance.

An Equal Opportunity Employer

Verona Pharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Verona Pharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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