Senior Clinical Project Manager

2 weeks ago

Dublin, Dublin City, Ireland Life Science Recruitment Full time

Direct message the job poster from Life Science Recruitment

Our client, a pharmaceutical company based in Dublin is currently recruiting for an experienced Senior Clinical Project Manager to join their team on a permanent basis. As Senior Clinical Project Manager, you will be responsible for the planning, execution, and management of clinical trials, ensuring compliance with regulatory requirements, budget, and timelines. You will have strong leadership skills, strategic thinking, and the ability to oversee the activity of different vendors, such as CROs and laboratories. Clinical trial management in the therapeutic areas of Gastrointestinal (GI) diseases and/or Oncology is highly desirable. This is an excellent opportunity to work directly with a sponsor organization.

Responsibilities:

  • Lead the planning and execution of clinical trials from initiation to completion
  • Develop and manage study budgets, timelines, and resources
  • Oversee protocol development, regulatory submissions, and sites selection
  • Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements
  • Act as the primary point of contact for internal and external stakeholders
  • Manage and mentor cross-functional teams, ensuring efficient communication and collaboration
  • Monitor study progress, identify risks, and implement mitigation strategies
  • Review and approve study-related documentation, including investigator brochures, informed consent forms, and clinical study reports
  • Provide strategic input into trial design, feasibility assessment, and operational strategy
  • Conduct regular project status updates and present findings to senior management

Requirements:

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field
  • Minimum of 5-7 years of experience in clinical trial management within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of clinical trial regulations (FDA, EMA, ICH-GCP)
  • Proven track record of managing multi-center, global clinical trials
  • Excellent project management, leadership, and problem-solving skills
  • Strong interpersonal and communication abilities to liaise with various stakeholders
  • Ability to work in a fast-paced, deadline-driven environment
  • Willingness to travel as needed
Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Science
  • Industries: Pharmaceutical Manufacturing and Biotechnology Research
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