Manager, Statistical Programming

5 - 9 years

11 - 15 Lacs

Posted:3 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

We are looking for a skilled Statistical Programmer with 5 to 10 years of experience in the pharmaceutical industry. The ideal candidate will have a strong background in statistical programming and analysis, with expertise in SAS, R, or other programming languages.
Roles and Responsibility
  • Develop and maintain complex statistical models and algorithms for data analysis.
  • Design and implement data visualizations to effectively communicate insights to stakeholders.
  • Collaborate with cross-functional teams to identify business needs and develop solutions.
  • Provide expert-level support for statistical programming activities, including data management and reporting.
  • Develop and maintain documentation of statistical models and procedures.
  • Ensure compliance with regulatory requirements and industry standards for statistical programming.
Job Requirements
  • Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences.
  • At least 5 years of programming experience in industry, with proficiency in SAS, R, or other programming languages.
  • Strong understanding of clinical data structure, relational database, and software tools like MS Office and XML.
  • Experience with Japan/PMDA submissions, eSub package (aCRF, SDRG, define.xml), and Pinnacle 21.
  • Excellent communication and collaboration skills, with the ability to work effectively in a team environment.
  • Demonstrated ability to handle and process upstream data, such as multiple data forms, workflow, eDC, and SDTM.
  • Proficiency in creating ADaM datasets and Data Definition Tables, and e-submission outputs.
  • Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs.
  • Ability to provide leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance, and corporate and departmental SOPs and work practices.
  • Identify opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors.
  • Independently lead and/or perform programming assignments with minimal supervision.
  • Support improvement initiatives.
Additional Info
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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Bristol Myers Squibb logo
Bristol Myers Squibb

Pharmaceutical Manufacturing

Lawrence Township NJ

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