Senior Clinical Leadership Opportunity

1 day ago

Dublin, Dublin City, Ireland beBeeClinical Full time €80,000 - €120,000
Clinical Scientific Expert Group Lead

This is an opportunity to excel as a Clinical Scientific Expert Group Lead. You will oversee a team of Clinical Scientific Experts, guiding their growth and development through coaching and mentoring. Your role will involve allocating resources, managing workload distribution, and ensuring that your team meets company objectives and priorities.

About the Role
  • Selects, recruits, develops, manages, motivates, coaches, and appraises direct reports to ensure high-quality performance and career development.
  • Manages resource assignments, workload distribution, and sharing within groups to meet company objectives and priorities.
  • Provides support to address and resolve issues, identifying solutions for remediation.
  • Builds a strong team culture focused on expertise, performance, and alignment with our values and behaviors.
  • Leads special projects, initiatives, and supports training programs for technical and professional skills within the team.
  • Acts as a Subject Matter Expert for key operational areas influencing the Clinical Scientific Expert Group and broader clinical development.
  • Collaborates with QA on audit readiness, regulatory inspections, and Health Authority compliance.
  • Promotes cultural change and integrates change management concepts aligned with our objectives, focusing on data-centric mindset and capability building.
Essential Requirements
  • Advanced degree in life sciences/healthcare preferred; experience in multinational organizations required.
  • >3 years experience in clinical study planning, execution, and publishing in industry/Academia, or 5+ years in Clinical Operations/Scientific roles; team/matrix management experience preferred.
  • Strong understanding of trial design principles (e.g., objectives, bias reduction, statistical methods, ethics) and clinical development processes, including GCP knowledge.
  • Thorough knowledge of clinical data collection/reporting systems (e.g., EDC tools, Rave, OC-RDC); ability to analyze trends and interpret/report data effectively.
  • Medical/scientific expertise with strong writing skills; capable of interpreting, discussing, and representing trial/program data.
  • Demonstrated leadership, planning, and people management skills, including mentoring/coaching within matrix environments.
  • Analytical background with proficiency in statistical methods; experience detecting data trends and escalating issues appropriately.
  • Strong interpersonal, communication, and problem-solving skills; ability to collaborate across boundaries for shared success.
Why Us

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Benefits

We offer a range of benefits and rewards to help you thrive personally and professionally.

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