Source description
About the role
Role Overview: As a Statistician at YouV Research, you will play a crucial role in conducting statistical analysis for clinical trials. You will be responsible for performing data cleaning, generating summary tables and listings, and assisting in the development of statistical analysis plans. Your role will involve collaborating with cross-functional teams to ensure data quality and integrity, as well as contributing to the interpretation of study results. Additionally, you will stay updated with relevant regulations and industry best practices to ensure the highest standards of statistical analysis. Key Responsibilities: - Assist in conducting statistical analysis for clinical trials. - Perform data cleaning and validation. - Generate summary tables, figures, and listings. - Assist in the development of statistical analysis plans and study protocols. - Collaborate with cross-functional teams to ensure data quality and integrity. - Contribute to the interpretation of study results. - Stay updated with relevant regulations and industry best practices. Qualifications Required: - Masters degree in Statistics, Biostatistics, or a related field. - Minimum of 1-2 years of industry experience as a Statistician within the Life Sciences industry or Contract Research Organization (CRO). - Experience in statistical analysis using SAS or R. - Familiarity with clinical trial protocols and statistical analysis plans. - Strong data interpretation and presentation skills. - Ability to work collaboratively in a team environment. Role Overview: As a Statistician at YouV Research, you will play a crucial role in conducting statistical analysis for clinical trials. You will be responsible for performing data cleaning, generating summary tables and listings, and assisting in the development of statistical analysis plans. Your role will involve collaborating with cross-functional teams to ensure data quality and integrity, as well as contributing to the interpretation of study results. Additionally, you will stay updated with relevant regulations and industry best practices to ensure the highest standards of statistical analysis. Key Responsibilities: - Assist in conducting statistical analysis for clinical trials. - Perform data cleaning and validation. - Generate summary tables, figures, and listings. - Assist in the development of statistical analysis plans and study protocols. - Collaborate with cross-functional teams to ensure data quality and integrity. - Contribute to the interpretation of study results. - Stay updated with relevant regulations and industry best practices. Qualifications Required: - Masters degree in Statistics, Biostatistics, or a related field. - Minimum of 1-2 years of industry experience as a Statistician within the Life Sciences industry or Contract Research Organization (CRO). - Experience in statistical analysis using SAS or R. - Familiarity with clinical trial protocols and statistical analysis plans. - Strong data interpretation and presentation skills. - Ability to work collaboratively in a team environment.