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