Global Clinical Program Lead

R&D Partners; Dublin; On-site; EUR 90,000 - 140,000; Full time

Job summary

R&D Partners seeks a Clinical Program Manager to lead global clinical programmes from early development to patients worldwide, ensuring regulatory compliance and high-quality study execution. You will oversee cross-functional SMTs, manage budgets, and guide CROs and vendors to meet milestones.

The ideal candidate has a strong background in clinical operations and study management, with leadership experience in a matrixed environment and the ability to travel as required.

Qualifications

• BA/BS or RN with 8+ years of relevant clinical experience in life sciences.
• MA/MS/PharmD/PhD with 6+ years of relevant experience.
• Minimum 4 years of cross-functional study management or leadership experience.

Responsibilities

• Oversee and manage clinical studies or programs, including financial oversight and resource allocation.
• Lead cross-functional Study Management Teams (SMTs) and collaborate with stakeholders to ensure project goals are met.
• Develop and manage project timelines, budgets, and risk mitigation strategies.
• Author and review study-related documentation, including protocols and regulatory submissions.
• Select, manage, and oversee contract research organizations (CROs) and vendors.
• Ensure compliance with international regulations, ICH guidelines, and GCP standards.
• Communicate project status.
• Participate in departmental or interdepartmental strategic initiatives.
• If assigned, manage a team of direct reports, providing coaching, development, and performance management.

Skills

Cross-functional leadership

Project management

Regulatory knowledge

Study coordination

Stakeholder communication

Education

BA/BS or RN

MA/MS/PharmD/PhD

Job description

R&D Partners seeks a Clinical Program Manager to lead global clinical programmes from early development to patients worldwide, ensuring regulatory compliance and high-quality study execution. You will oversee cross-functional SMTs, manage budgets, and guide CROs and vendors to meet milestones.

The ideal candidate has a strong background in clinical operations and study management, with leadership experience in a matrixed environment and the ability to travel as required.