Clinical Program Manager

  • Dublin
  • Contract

Position: Clinical Program Manager

Location: Dublin, Ireland

Contract Length: 12-month (View to extend)

Work Structure: Monday - Friday (on-site)

Pay Rate: Available on request

Are you a seasoned Clinical Program Manager who is looking to be involved to expand on their expertise? If so, this opportunity is what you need!

This client is a biopharmaceutical company, that is globally known for developing and commercializing innovative medicines in areas with unmet medical needs - Such as: HIV/AIDS, Hepatitis, Oncology, as well as Inflammatory and Respiratory Diseases.

Clinical Program Manager - Responsibilities:

The new Clinical Program Manager will work with the Clinical Trial Manager and study teams to manage studies within a program and across all regions, providing a significant role in oversight and management of programs, leading cross-functional teams, driving performance and ensuring consistent execution of delivery.

  • Provides guidance and oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
  • Provides Clinical Operations therapeutic area leadership.
  • Accountable for successful study completion including clinical trial budgets and timelines.
  • Leads cross-functional study management teams and should have good influencing skills with study stakeholders.
  • Ensures consistent execution of program requirements across studies in a program.
  • Manages study resources and responsible for career development and guidance of direct reports.
  • Partners with functional peers to manage, adjust, and revise project timelines/budgets as necessary.
  • Writes study protocols, study reports, sections for investigator brochures and regulatory documents (e.g. IND, NDA, etc.) with little supervision.
  • Develops and progresses RFPs and selection and management of CROs/vendors.
  • Travel is required.

Clinical Program Manager - Knowledge, Experience & Skills:

  • BSc or BA in a relevant scientific discipline or RN qualification.
  • At least seven years relevant clinical trial experience in the pharmaceutical industry.
  • Ability to manage and motivate teams and drive performance.
  • Ability to develop study team members.
  • Must have a demonstrated ability to successfully develop, implement, manage, and complete clinical trials.
  • Must have functional expertise to initiate, author, or contribute to SOP development, implementation, and training.
  • Knowledge of FDA and/or EMEA Regulations, ICH Guidelines and GCP governing the conduct of clinical trials.

If you have the experience required for this challenging yet rewarding role, please submit your application including a CV and cover letter to or press the "Apply" button below.

Jordon Manzo Senior Candidate Consultant I

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