Statistician 1

Posted Yesterday
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Bengaluru, Bengaluru Urban, Karnataka, IND
In-Office
Junior
Healthtech • Biotech
The Role
Perform SAS programming and statistical analyses for clinical study data, prepare report sections, QC teammates' work, maintain project documentation, and ensure compliance with GLP/GMP/GCP while liaising with internal clients.
Summary Generated by Built In

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives.


Labcorp is seeking a Statistical Analyst to join our team at Labcorp, Bangalore office, Yeshwantpur

Work Schedule

2nd shift (2PM - 11PM)

Job Responsibilities
  • Liaise with internal clients, as required, regarding the requirements for analysis of study data.

  • Assist in developing SAS library code for use by the Statistics department.

  • Responsible for Statistics deliverables within assigned projects.

  • Perform quality control (QC) of team members' work.

  • Conduct statistical analysis of study data and support related decision-making.

  • Prepare sections of statistical reports and study reports.

  • Maintain the overall status and quality of Statistics project documentation, including hardcopy and electronic files.

  • Perform SAS programming and related activities for the presentation and analysis of study data.

  • Conduct all work in compliance with applicable regulatory requirements, including GLP, GMP, and GCP, as specified in study plans, protocols, or work agreements.

  • Ensure the quality and accuracy of personal work.

  • Perform other duties as assigned by management.

Minimum Qualifications
  • Master's degree in Statistics or a related field.

  • 1 to 3 years of postgraduate experience applying statistics in a pharmaceutical or life sciences environment.

  • Proficiency in SAS programming, including the use of a variety of statistical procedures.

  • Experience with statistical methodology, analysis, and reporting.

  • Ability to adhere to strict guidelines, regulatory requirements, and codes of practice.

  • Strong interpersonal, communication, and organizational skills.

  • Self-motivated with the ability to work independently and collaboratively.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.


Skills Required

  • Master's degree in Statistics or a related field.
  • 1 to 3 years postgraduate experience applying statistics in a pharmaceutical or life sciences environment.
  • Proficiency in SAS programming, including use of various statistical procedures.
  • Experience with statistical methodology, analysis, and reporting.
  • Ability to adhere to strict guidelines, regulatory requirements, and codes of practice (GLP, GMP, GCP).
  • Strong interpersonal, communication, and organizational skills.
  • Self-motivated with ability to work independently and collaboratively.
  • Ability to perform quality control of team members' work and maintain project documentation.
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The Company
HQ: Burlington, NC
19,796 Employees
Year Founded: 1978

What We Do

We believe in harnessing science for human good. And so we work day and night, around the world, to deliver answers for all your health questions—whether you’re a provider, drug developer, hospital, medical researcher or patient. That means everything from advancing diagnostic testing to helping launch new drugs, to offering new perspectives through data - all drawing from a deep well of scientific expertise. So when you need trusted information to make clear, confident health decisions, consider us your source.

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