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Job summary
A leading global healthcare consultancy is seeking a professional to manage Significant Quality Events within clinical development. The role involves forming and leading event teams, conducting investigations, and ensuring all documentation adheres to regulatory standards. Candidates should possess a degree in a drug-related discipline, with strong project management and communication skills, along with 3-5 years of relevant experience. The position is located in Groton, Connecticut, offering an exciting opportunity to influence quality management processes.
Qualifications
3-5 years of experience in quality management.
Understanding of clinical trials and regulatory requirements.
Ability to influence global stakeholders.
Responsibilities
Manage Significant Quality Events.
Form Significant Quality Event Teams.
Conduct Root Cause Analysis and document outcomes.
Skills
Project management
Interpersonal skills
Communication skills
Root Cause Analysis
Education
Degree in related discipline
Job description
A leading global healthcare consultancy is seeking a professional to manage Significant Quality Events within clinical development. The role involves forming and leading event teams, conducting investigations, and ensuring all documentation adheres to regulatory standards. Candidates should possess a degree in a drug-related discipline, with strong project management and communication skills, along with 3-5 years of relevant experience. The position is located in Groton, Connecticut, offering an exciting opportunity to influence quality management processes.