Study Manager, Clinical Operations

The Clinical Operations Clinical Study Manager will be accountable for managing the clinical operations activities for approximately 2 to 3 clinical trials, driving strategic clinical trial operational planning, and ensuring patient safety and data integrity.

Requirements

• BSc in Life Sciences with four (4) years of experience working in Pharma/Biotech, experience in rare disease areas, pediatric studies, and/or gene therapy
• Excellent organizational and communication skills
• Detail oriented
• ‘Can-do’ attitude and willingness to be flexible
• Demonstrated leadership skills
• Demonstrated collaborative style of working
• Fluent business English (oral and written)
• Experience and knowledge of clinical study/project management
• Experience in oversight of service providers (e.g. CROs, central and specialty labs, etc.)
• Experience leading a clinical trial with a cross functional team
• Understanding of regulatory environment, GCP/ICH and compliance requirements for clinical research

Benefits

• Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship
• Generous Parental Leave