I use SAS to extract, transform, and load data into the database and ensure data quality and completeness. I have experience working with clinical databases such as Oracle Clinical and Medidata Rave. Can you explain your experience working with clinical databases? Automation and macros help to reduce programming errors and save time. Additionally, I have experience in creating custom macros to solve specific programming challenges. I have experience in automating repetitive programming tasks using SAS macros. Can you explain your experience with automation and macros in programming? Additionally, I collaborate with the clinical team to identify and resolve data discrepancies. I perform quality checks during the data cleaning and analysis phase to ensure data integrity, completeness, and accuracy. How do you ensure data quality in clinical trials?ĭata quality is crucial in clinical trials, and I ensure it by following standard operating procedures (SOPs) and guidelines. Additionally, I have experience in creating Tables, Listings, and Figures (TLFs) and have worked with data from various therapeutic areas. I am familiar with clinical trial data standards such as CDISC and SDTM and use SAS to clean, analyze and report clinical trial data. I have extensive experience working with SAS in a clinical trial setting. What experience do you have working with SAS in a clinical trial setting? Additionally, I used Python and R for data visualization and statistical analysis. In my previous role, I used SAS to clean and analyze clinical trial data, and SQL to extract data from databases. I am proficient in languages such as SAS, SQL, Python, and R. What programming languages are you proficient in, and how have you used them in your previous role? Can you explain your experience working with clinical data from various therapeutic areas?.How do you handle missing data in a clinical trial analysis?.

Can you explain your experience with CDISC standards and ADaM datasets?.How do you ensure confidentiality and data security in clinical trials?.Can you give an example of a complex statistical analysis you have conducted in a clinical trial?.Can you explain your experience in creating clinical study reports (CSRs)?.How do you ensure compliance with regulatory guidelines in clinical trials?.How do you manage timelines and prioritize tasks in a fast-paced clinical trial environment?.Can you explain your experience working with clinical databases?.

Can you explain your experience with automation and macros in programming?.

How do you ensure data quality in clinical trials?.

What experience do you have working with SAS in a clinical trial setting?.

What programming languages are you proficient in, and how have you used them in your previous role?.

Oncology sas interview questions