Clinical Supply Specialist

ICON Clinical Research, LP

Dublin, Ireland
Not specified; competitive within country; range o...
Fully remote
3 years relevant clinical supply experience
Knowledge of ich/gcp regulatory guidelines
Proficiency with ms word and excel
ICON Clinical Research is seeking a Clinical Supply Specialist to manage and coordinate clinical supplies activities for clinical trials. The ideal candidate will have relevant experience in clinical supply management, particularly within the biotechnology or pharmaceutical sectors, and will thrive in a supportive and inclusive work environment

Job Summary

  • The role involves managing and coordinating clinical supplies activities to support the successful execution of clinical trials at ICON.
  • Candidates will be responsible for inventory tracking, shipment orders, temperature excursion evaluation, and expiry management for investigational products.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Supply Specialist to manage and coordinate clinical supplies activities for clinical trials. The ideal candidate will have relevant experience in clinical supply management, particularly within the biotechnology or pharmaceutical sectors, and will thrive in a supportive and inclusive work environment.

Salary

Not specified; Competitive within country; Range of additional benefits offered

Skills & Requirements

Must-have

  • 3 years relevant clinical supply experience
  • Knowledge of ICH/GCP regulatory guidelines
  • Proficiency with MS Word and Excel
  • Experience in biotechnology or pharmaceutical industry
  • Strong problem-solving and time management skills

Nice-to-have

  • Action-oriented with high agility and adaptability
  • Excellent organizational and detail-oriented approach
  • Collaborative communication across functional groups
  • Experience with process initiatives and metrics tracking

Key Requirements

  • Bachelor's Degree required
  • At least 3 years of relevant experience in Clinical Supplies, QA/Regulatory, Supply Chain, or Manufacturing
  • Fundamental knowledge of International Council of Harmonization (ICH) / Good Clinical Practices (GCP)

Work Rights

Not specified

Tailored Resume

Cover Letter