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Job Description

  • Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
  • At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
  • Statistical Programming and SAS hands-on experience
  • Clinical trials expertise with a thorough understanding of data operations required for the reporting of clinical trial data.
  • Good understanding of ICH and Regulatory Guidelines
  • Routine problem-solving skills, developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.
  • Thorough understanding of clinical data and relevant data standards
  • Extensive knowledge of routine statistical methodology and its application to programming
  • Knowledge of vendor processes
  • Demonstrated experience in developing successful partnerships within study teams
  • Strong written and oral communication skills, and project management skills
  • Ability to present technical information to a non-technical audience
  • Proven ability to operate independently.
  • Some exposure working across international boundaries and cultures.
  • Ability to manage customer expectations.
  • Ability to manage work of others in a remote and/or global setting
  • CDISC experience highly desirable.
  
Work Location Assignment: Flexible

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.


Medical#LI-PFE

Job Details

Job Location
India
Company Industry
Other Business Support Services
Company Type
Unspecified
Employment Type
Unspecified
Monthly Salary Range
Unspecified
Number of Vacancies
Unspecified

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