Clinical Program Manager (CPM)

R Dpartners; Dublin; On-site; EUR 69,000 - 86,000; Full time

Job summary

R Dpartners is seeking a Clinical Program Manager (CPM) to lead global clinical programmes from early development through patient access in ROI. You will oversee study management, budgets, timelines, and CRO oversight, ensuring compliance with ICH and GCP across therapeutic areas.

Ideal candidates have 6+ years in clinical operations or study leadership, strong collaboration skills, and the ability to travel as required. This role commands a competitive hourly rate in ROI.

Qualifications

• 8+ years of clinical experience in life sciences or 6+ years with advanced degrees.
• Experience leading cross-functional study management teams.
• Strong regulatory knowledge and document authoring skills.

Responsibilities

• Oversee and manage clinical studies or programs with budgets and resources.
• Lead cross-functional SMTs and coordinate with stakeholders to meet goals.
• Develop timelines, budgets, risk plans, and report progress.
• Author study documentation and manage CROs/vendors and regulatory submissions.

Skills

Clinical program management

Cross-functional leadership

Regulatory/compliance knowledge

Education

BA/BS/RN with 8+ years of clinical experience

MA/MS/PharmD/PhD with 6+ years of experience

Tools

FDA/EMA/ICH/GCP regulations

Job description

Ready to lead global clinical programmes that bring innovative therapies from early development to patients worldwide?

R&D Partners is seeking a Clinical Program Manager (CPM) to join a leading pharmaceutical company in ROI. This role focuses on the successful execution of clinical trials across all phases (I-IV) and therapeutic areas, ensuring compliance with regulatory guidelines and company policies. The ideal candidate will have a strong background in clinical operations, study management, and cross-functional leadership.

Please note that to be considered for this role you must have the right to work in this location.

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, elevate issues, and implement solutions to achieve project goals.
• Participate in departmental or interdepartmental strategic initiatives.
• If assigned, manage a team of direct reports, providing coaching, development, and performance management.

Key Skills and Requirements

Education & Experience

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

Technical Expertise

• Advanced knowledge of disease or therapeutic areas and full-cycle study management.
• Proficiency in developing RFPs, managing CROs/vendors, and authoring clinical study documentation.
• Thorough understanding of FDA, EMA, ICH, and GCP regulations.

Leadership & Communication

• Proven ability to lead and influence teams in a matrixed environment.
• Strong interpersonal, organizational, and change management skills.
• Demonstrated effectiveness in coaching and developing team capabilities.

Other Requirements

• Ability to travel as required.

Salary

• €50 – €62.30/Hr

For more information, please contact Mandi Cakwe.