The Clinical Trial Support Manager supports the clinical study leader in executing studies, managing budgets, and ensuring regulatory compliance
Job Summary
The Clinical Trial Support Manager supports the clinical study leader in executing studies, managing budgets, and ensuring regulatory compliance.
Responsibilities include developing study documents like risk management plans, overseeing vendor activities, and managing investigational medicinal product logistics.
Candidates must possess a bachelor's degree in a scientific field and at least two years of experience in clinical operations with knowledge of FDA and EMA regulations.
Matching Summary
The Clinical Trial Support Manager supports the clinical study leader in executing studies, managing budgets, and ensuring regulatory compliance.
Skills & Requirements
Must-have
Bachelor's degree in scientific discipline
2 years clinical operations experience
Knowledge of GCP and ICH guidelines
Study risk management plan development
Budget tracking and invoice approval
Vendor management and performance oversight
Sample collection and analysis monitoring
Nice-to-have
Critical thinking and problem-solving mindset
Ability to work autonomously with cross-functional teams
Experience with centralized monitoring strategies
Fluency in English for international meetings
Proactive issue escalation and resolution skills
Adaptability to new digital tools and processes
Key Requirements
Bachelor's degree (advanced preferred)
Minimum 2 years clinical operations experience
Understanding of GCP, ICH, FDA, and EMA regulations
Strong written and verbal communication skills in English