Clinical Data Reporting Specialist

The Clinical Data Reporting Specialist will be responsible for supporting pharmaceutical research and development through clinical data analysis, reporting, and business intelligence solutions. The specialist will utilize SAS (or equivalent) software for data extraction, transformation, and loading (ETL), conduct statistical analyses, and generate regulatory-compliant reports. The role requires collaboration with cross-functional teams to ensure data integrity, compliance with industry standards, and timely delivery of clinical insights. JOB DUTIES: Perform data extraction, transformation, and loading (ETL) processes using SAS (or equivalent) software. Develop and execute SAS (or equivalent) programs for statistical analysis and clinical data reporting. Generate standard and ad-hoc reports to support clinical trials and regulatory submissions. Validate clinical data to ensure accuracy, completeness, and compliance. Collaborate with cross-functional teams to interpret data and provide analytical insights. Utilize Business Intelligence (BI) tools to visualize and communicate clinical data trends. Ensure compliance with applicable regulatory guidelines, including FDA requirements. Contribute to improving data management practices and standard operating procedures (SOPs). RELOCATION REQUIREMENTS: Relocation to various unanticipated client sites across USA required up to 4 times per year. MINIMUM REQUIREMENTS:

Education: Bachelor’s degree or foreign equivalent in Clinical Informatics, Health Informatics, Pharmaceutical Sciences, Clinical Analytics, or a related field. Knowledge, Skills, and Abilities (KSAs): Must have knowledge, skills, and abilities in the following (can be gained through education, training, or experience): Proficiency in SAS (or equivalent) software for clinical data manipulation, statistical analysis, and reporting. Knowledge of clinical data management principles and pharmaceutical industry standards. Understanding of statistical methodologies and clinical trial processes. Familiarity with regulatory guidelines (e.g., FDA) for clinical data reporting and compliance. Ability to interpret and present complex clinical data effectively. Use of Business Intelligence (BI) tools (e.g., Tableau, Power BI) for data visualization. Excellent communication and collaboration skills in cross-functional environments. Organizational and time management skills to meet regulatory deadlines. Ability to follow standard operating procedures and regulatory protocols. Minimum Requirements Apply To The Positions Listed Above. Please Refer To This Advertisement. No Phone Calls Please. Equal Opportunity Employer. Please Mail Your Resume To: HR Manager Ursi Technologies, Inc. 5440 McGinnis Village Place, Suite 102 Alpharetta, GA 30005