Clinical Specialist - General Medicine

Job Description

Job Summary

The Clinical Specialist position is a combined position of clinical scientist and study management duties supporting one or more clinical trials. Under the oversight of a clinical scientist, study manager, or program lead, the Clinical Specialist may be responsible for but not limited to:

Job Responsibilities

• Maintain clinical trial files (including eTMF), project processes, tracking systems, and other utilized study or departmental systems
• Generating and reviewing medical monitoring reports
• Creating and maintaining project schedules
• Distributing, reconciling, and archiving clinical documents
• Tracking and reconciling labs/samples
• May interact with internal and external stakeholders (e.g., study sites, committees) in support of clinical trial objectives

Core Skills

• Pharmaceutical, research, medical, and/or clinical drug development knowledge/experience
• Strong communication, writing, and presentation skills
• Effective time management and organizational skills
• Ability to effectively work in a team environment and independently
• Proficient knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
• Preferred: knowledge of GCP, project management, process improvement, data analytics

Education/Experience

• Bachelor's Degree +1 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree
• Degree in life sciences, preferred.

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