Associate Director, Clinical Programs 
 

Responsible for oversight, coordination, and execution of clinical studies in support of clinical programs. This role combines hands on trial management with program level operational leadership to ensure studies progress efficiently and deliver against program objectives.

Education/Skills and Experience Requirements:
  • Science background BS or healthcare degree required, Masters preferred.
  • Experience:10+ years (or equivalent senior-level experience) in clinical research experience in a pharmaceutical/biotech, CRO setting; monitoring experience a plus.
  • Strong knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials.
  • Strong leadership, interpersonal, organizational, and multitasking skills.
  • Excellent attention to detail and problem solving skills.
  • Ability to work effectively work in a team setting.



 

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