As a Biostatistics Manager at our organization, you will play a pivotal role in managing and supervising a team of statisticians and biostatisticians. Your responsibilities will include overseeing statistical analysis and reporting activities for clinical trials, providing guidance on study design, sample size estimation, and statistical methodologies, as well as collaborating with cross-functional teams to ensure timely and accurate deliverables while maintaining compliance with regulatory guidelines and industry standards. In this role, you will be required to manage and allocate resources within the biostatistics team, ensuring adherence to quality and regulatory standards in statistical analysis. You will also collaborate with project teams to develop statistical analysis plans, oversee the preparation of statistical deliverables for regulatory submissions, provide guidance on complex statistical issues and study interpretations, and foster a culture of continuous learning and professional development within the team. To qualify for this position, you should have a Master's degree or Ph.D. in Statistics, Biostatistics, or a related field, along with a minimum of 8-10 years of progressive experience in Biostatistics, including leadership roles, within the pharmaceutical, biotechnology, or CRO industry. You should possess extensive experience in statistical analysis and clinical trial research, strong leadership and management skills, excellent communication and presentation abilities, and the ability to collaborate effectively with cross-functional teams. Join us in our mission to make work meaningful together, where alternative thinking gives rise to innovative ideas and human-centric processes are created through teamwork, co-creation, and co-execution. At YouV, you can expect unparalleled exposure, valuable learning opportunities, and a positive work environment that will add great value to your career. Immerse yourself in our unique culture of warmth and positivity, where collaboration, open-door policies, and inclusivity are at the core of everything we do.,
As a Senior Statistician at our organization, you will play a crucial role in overseeing statistical analysis activities across multiple clinical trials. Your expertise will be instrumental in providing expert statistical guidance to project teams and stakeholders, ensuring the development of innovative statistical methodologies, and contributing to research publications. Your leadership skills will be put to test as you lead the preparation of statistical deliverables for regulatory submissions and mentor junior statisticians, providing them with training and professional development opportunities. In this role, you will be responsible for leading and managing statistical analysis projects, conducting complex statistical analyses, and interpreting critical data. You will guide the development and review of study protocols and statistical analysis plans, ensuring compliance with regulatory requirements and industry standards. Collaboration with cross-functional teams and external partners will be essential, along with staying updated with emerging statistical methodologies and industry trends. Your participation in business development activities, such as proposal development and client presentations, will be key to the growth and success of our organization. Join us in creating meaningful work together, where your skills and experience will be valued and where you will have the opportunity to make a significant impact in the field of biostatistics.,
As an Associate Statistician at our organization, your role will involve assisting in conducting statistical analysis for clinical trials. You will be responsible for performing data cleaning and validation, as well as generating summary tables, figures, and listings. Additionally, you will collaborate with cross-functional teams to ensure data quality and integrity, contribute to the interpretation of study results, and stay updated with relevant regulations and industry best practices. Your qualifications should include a Bachelor's degree in Statistics, Biostatistics, or a related field. You will have the opportunity to work under the guidance of senior statisticians, conduct statistical analysis, perform data management tasks such as data cleaning and transformation, and assist in generating analysis datasets and statistical outputs. Collaboration with programmers and data managers to ensure data quality and consistency will also be a key part of your responsibilities. Furthermore, you will contribute to the development and review of study documents and regulatory submissions, participate in departmental meetings and training programs, and stay informed about emerging statistical methodologies and industry trends. Our organization values teamwork, co-creation, and co-execution, providing a supportive and inclusive work environment where you can learn and grow beyond your designated role. Join us in making work meaningful together and be a part of a culture that promotes warmth, positivity, and collaboration.,
As a Statistician I at YouV, you will play a crucial role in conducting statistical analysis for clinical trials, contributing to the interpretation of study results, and ensuring data quality and integrity. Your responsibilities will include: - Assisting in statistical analysis for clinical trials. - Performing data cleaning and validation. - Generating summary tables, figures, and listings. - Assisting in the development of statistical analysis plans and study protocols. - Collaborating with cross-functional teams to ensure data quality and integrity. - Contributing to the interpretation of study results. - Staying updated with relevant regulations and industry best practices. Qualifications required for this role include: - Education: Masters degree in Statistics, Biostatistics, or a related field. - Experience: Minimum of 1-2 years of industry experience as a Statistician within the Life Sciences industry or Contract Research Organization (CRO). - Proficiency 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. Join us at YouV and be part of a collaborative, open-door, and inclusive environment where you will have the opportunity to learn beyond your designation and grow your skills. Experience a unique blend of warmth, positivity, and professional development.,