Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office

Syneos Health, Inc.

Dublin

Hybrid

EUR 120,000 - 180,000

Full time

5 days ago
Be an early applicant
Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Job summary

Syneos Health, Inc. seeks a Single Sponsor Associate Clinical Project Director (Program Manager) to lead end-to-end clinical study management with a focus on delivering quality results.

The role involves managing study teams, coordinating with functional groups, and ensuring alignment with project goals in a dynamic sponsor environment. The position requires extensive experience in Clinical Operations, with strong leadership and vendor management capabilities, in a CRO or pharmaceutical setting.

Qualifications

  • End-to-end program management experience in clinical trials.
  • Solid background in Clinical Trial Management or Clinical Project Management.
  • Cross-functional study management leadership in CRO or Pharma.

Responsibilities

  • Oversee execution of studies within a program with financial responsibility.
  • Lead study teams and manage resource deployment for a fluid One Ops workforce.
  • Manage vendor oversight and stakeholder relationships at the study level.

Skills

End-to-end program management
Clinical trial management
Leadership

Education

BA / BS / RN

Job description

Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office

Updated: September 24, 2026
Location: Dublin 2, Ireland
Job ID:25111867

Description

Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:

Why Syneos Health
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
  • Typically manages a team of direct reports and may have indirect reports. Plays a leadership role in team member recruitment, on-boarding and leads ongoing training and coaching of team members.
  • May provide input into strategic and operational short- and long-range therapeutic area / functional area plans as appropriate, including supporting alignment and communications to other team members upon implementation.
  • Champions Values and Leadership Commitments.
  • Responsible for overseeing the successful execution of studies and/or multiple studies within a program or multiple programs, including financial responsibility.
  • Responsible for leading or otherwise overseeing study teams related to assigned studies.
  • Proactively manages vendor engagement for appropriate third-party oversight at the study-level, including proactive governance.
  • Proactively manages stakeholder relationships at the study-level.
  • Proactively manages oversight of clinical study execution, including developing operational strategies for the study to optimize execution.
  • May actively contribute to and/or represent Clinical Operations at sub-teams as applicable, including providing input and support to Associate Directors / Directors as needed.
  • Acts as a manager of managers and individual contributors with a People First approach that focuses on employee engagement, development and team health.
  • Responsible for the resource management of assigned studies, including an ongoing assessment of resource needs and optimal deployment of resources to support a fluid ‘One Ops’ workforce.
  • Effectively participates and engages in Clinical Operations and/or cross-functional change initiatives.
  • Leads and/or engages in Clinical Operations-specific change initiatives, typically therapeutic area- or functional area- specific.
  • May have business process owner (BPO) responsibilities and/or serve as a subject matter expert for Clinical Operations processes.
  • Encourages an innovative mindset by championing new ideas and initiatives that incorporate best practices, external benchmarking and standardization across Clinical Operations.
  • Ensures team’s work complies with established practices, policies and processes, and any regulatory or other requirements.
  • Experience needed.
  • BA / BS / RN with end to end program management experience, with a solid background in Clinical Trial Management or Clinical Project Management.
  • Operating at a high level in a cross-functional study management or related leadership experience in CRO or Pharma, including multiple years’ experience leading and managing study management or project teams.
Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Summary

Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across therapeutic areas. Clinical Operations plays a key role in ensuring all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of our client's products.This individual will manage a team of direct and potentially indirect reports. Oversee and be responsible for the successful execution of studies and/or multiple studies within a program or multiple programs, including financial responsibility. You may act as the business process owner (BPO) and/or serve as a subject matter expert for Clinical Operations processes.You will encourage an innovative mindset by championing new ideas and initiatives and incorporating best practices, external benchmarking and standardization across Clinical Operations.

Discover what our more than 29,000 employees already know: work here matters everywhere. We work hard,and smart, all in the name of getting much-needed therapies to thosewho need them most. A career with Syneos Health means your everyday work improvespatients’ lives around the world. Selecting us as an employer secures a career inwhich you’re guaranteed to:

Syneos Health ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office
Single Sponsor Associate Clinical Project Director (Program Manager) - 3 days in the Dublin office

Syneos Health • Dublin

On-site
EUR 110,000 - 140,000
Senior Clinical Program Director, Sponsor Studies (Dublin)
Senior Clinical Program Director, Sponsor Studies (Dublin)

Syneos Health • Dublin

Hybrid
EUR 110,000 - 140,000
Senior Clinical Program Director - Dublin Office
Senior Clinical Program Director - Dublin Office

Syneos Health, Inc. • Dublin

Hybrid
EUR 120,000 - 180,000
Clinical Program Manager (CPM)
Clinical Program Manager (CPM)

R&D Partners • Dublin

On-site
EUR 90,000 - 140,000
Clinical Program Manager (CPM)
Clinical Program Manager (CPM)

R Dpartners • Dublin

On-site
EUR 69,000 - 86,000
Global Clinical Operations AI Program Associate Director
Global Clinical Operations AI Program Associate Director

Novartis Ireland • Dublin

On-site
EUR 89,000 - 166,000
Hybrid working
Insurance plans
Retirement plans
+1
Sr. Associate / Manager - Clinical Development Trial Lead (Cardiometabolic Health)
Sr. Associate / Manager - Clinical Development Trial Lead (Cardiometabolic Health)

Eli Lilly and Company • Cork

On-site
EUR 70,000 - 100,000
Global Clinical Operations AI Product Director
Global Clinical Operations AI Product Director

Novartis Ireland • Dublin

On-site
EUR 102,000 - 190,000
Insurance plans
Retirement plans
Wellbeing resources
+3
Director Programme Operation -Oncology.
Director Programme Operation -Oncology.

Back4good • Cork

On-site
EUR 80,000 - 100,000
Director, Clinical Fsp Go To Market/Therapeutic Strategy Lead
Director, Clinical Fsp Go To Market/Therapeutic Strategy Lead

IQVIA • Dublin

Remote
EUR 120,000 - 180,000