Sr Clinical Data Associate

As a Sr Clinical Data Associate, you will be responsible for managing and analyzing clinical trial data to support the development of new medical products. This role will involve working closely with cross-functional teams to ensure data quality, integrity, and compliance with regulatory requirements. You will be responsible for designing, implementing, and maintaining data management systems, as well as developing and executing data analysis plans to support clinical trials. The ideal candidate will have experience with data management tools such as SAS and SQL, as well as strong analytical and problem-solving skills.

Key Responsibilities:

• Design, implement, and maintain data management systems to support clinical trials.
• Develop and execute data analysis plans to support clinical trials.
• Ensure data quality, integrity, and compliance with regulatory requirements.
• Collaborate with cross-functional teams to ensure data is accurate and complete.
• Develop and maintain data visualizations and reports to support business decisions.

Requirements:

• 5+ years of experience in clinical data management.
• Strong experience with data management tools such as SAS and SQL.
• Experience with data analysis and statistical software such as Python.
• Strong analytical and problem-solving skills.
• Ability to work in a fast-paced environment and prioritize multiple tasks.