Senior Statistical Programmer Catalyst Clinical Research

5.0 - 9.0 years

0 Lacs

thiruvananthapuram, kerala

On-site

As a SAS Programmer at Catalyst Clinical Research, you will play a crucial role in providing SAS programming support for Statistics and Data Management functions related to clinical trials and regulatory submissions. Your responsibilities will involve collaborating closely with Biostatisticians and Data Managers to develop SAS programs for validating tables, listings, and figures, as well as assisting with data cleaning and query generation. Additionally, you will serve as a contact for programming activities within the organization. Key Responsibilities: - Perform data manipulation techniques and advanced programming techniques such as arrays, transpositions, complex merges, SQL, SDTM, etc., and develop generic macros for generating listings, tables, and graphs. - Engage in statistical programming and validation of CDISC SDTM, Analysis Datasets (ADaM), and Tables, Listings, Graphs (TLGs). - Analyze information to devise innovative solutions for programming and data analysis challenges. - Produce high-quality results efficiently within specified time constraints. - Coordinate multiple priorities successfully and lead statistical programming activities on internal project teams. - Assist in identifying project priorities, communicating timelines, and ensuring the efficiency and quality of data reporting. - Represent the department in client meetings/presentations and maintain positive relationships with sponsors and collaborators. - Contribute to the ongoing improvement of programming processes and methodologies. - Provide guidance and advice to junior programmers, adapt to changing priorities, and fulfill ad hoc requests while performing high-level reviews on deliverables. Qualifications Required: - MSc in Biostatistics, Statistics, Computer Science, or a related field. - 5-7 years of experience in leading statistical programming activities in clinical research. - Preferred certification as a SAS Certified Candidate. - Good understanding of Clinical Trials and relevant terminologies. - Previous experience in pharmaceutical research or CRO setting. - Proficiency in statistical software packages, with a preference for SAS, and hands-on experience in developing SDTM datasets. - Strong verbal and written communication skills. - Positive attitude, willingness to learn, contribute to a team setting, and ability to successfully lead a single project. Visit CatalystCR.com to learn more about Catalyst Clinical Research and how your role as a SAS Programmer contributes to advancing clinical studies.,

Posted 1 day ago

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Biostatistics - Statistician I YOUV Research

1.0 - 5.0 years

0 Lacs

karnataka

On-site

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.,

Posted 4 days ago

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Biostatistics - Associate Statistician YOUV Research

1.0 - 5.0 years

0 Lacs

bangalore, karnataka

On-site

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.,

Posted 6 days ago

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