The Clinical Information System Analyst will support clinical trials through the development and optimization of reporting solutions, enabling data-driven problem-solving within a regulated environment (GCP, GCDMP, FDA guidelines). The Analyst will work closely with cross-functional teams to manage clinical data, design analytics, and ensure quality and compliance standards are met. This role requires strong communication, analytical, and project management skills.

Key Responsibilities:

• Develop and optimize clinical data reports and dashboards.
• Analyze clinical trial data using relational databases and advanced programming tools.
• Support data collection best practices for clinical trials.
• Manage multiple projects and ensure alignment with quality and regulatory requirements.
• Communicate findings clearly to stakeholders across different levels.

Hard Requirements:

• Proficiency in Tableau and/or Power BI.
• Strong experience with DAX, SQL, Python, or R programming.
• Expertise in Data Analytics/Data Science and Relational Databases (preferably Oracle RDBMS).
• Minimum of 2 years of relevant experience in clinical research or data analytics.
• Bachelor's degree in Business Administration, Data Science, Statistics, or Life Sciences.

Preferred Qualifications:

• Experience with SSRS.
• Strong understanding of clinical trial data management practices.
• Ability to manage multiple projects in a regulated, quality-focused environment.