What are the responsibilities and job description for the Study Execution and Management Specialist position at Regeneron Pharmaceuticals?
Job Details
The Senior Manager Global Study Execution is an exciting opportunity to join a dynamic team and contribute to the success of our clinical trials. As a key member of our operations team, you will be responsible for leading the execution of large and complex studies, working closely with cross-functional teams to ensure timely and successful study execution. This role requires strong leadership and project management skills, as well as excellent communication and problem-solving abilities.
Key Responsibilities:
• Oversee the development and implementation of study-specific documentation, including case report forms, data management plans, and monitoring plans
• Collaborate with cross-functional teams to ensure timely and successful study execution
• Identify and mitigate risks associated with study execution
• Develop and implement patient recruitment and retention strategies
• Monitor data entry and query resolution, and escalate issues to program operations leader and other stakeholders as needed
Requirements:
• Minimum 8 years of relevant industry experience
• Bachelor's degree or equivalent
• Strong project management and leadership skills
• Excellent communication and problem-solving abilities
• Experience with clinical trial management systems and MS applications
The Senior Manager Global Study Execution is an exciting opportunity to join a dynamic team and contribute to the success of our clinical trials. As a key member of our operations team, you will be responsible for leading the execution of large and complex studies, working closely with cross-functional teams to ensure timely and successful study execution. This role requires strong leadership and project management skills, as well as excellent communication and problem-solving abilities.
Key Responsibilities:
• Oversee the development and implementation of study-specific documentation, including case report forms, data management plans, and monitoring plans
• Collaborate with cross-functional teams to ensure timely and successful study execution
• Identify and mitigate risks associated with study execution
• Develop and implement patient recruitment and retention strategies
• Monitor data entry and query resolution, and escalate issues to program operations leader and other stakeholders as needed
Requirements:
• Minimum 8 years of relevant industry experience
• Bachelor's degree or equivalent
• Strong project management and leadership skills
• Excellent communication and problem-solving abilities
• Experience with clinical trial management systems and MS applications
