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14 Cytel Statistical Software & Services Jobs
Senior Statistical Programmer FSP
8-9 years
Kolkata, Mumbai, New Delhi + 4 more
1 vacancy
Senior Statistical Programmer FSP
Cytel Statistical Software & Services
posted 3+ weeks ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
- We believe in applying scientific rigor to reveal the full promise inherent in data.
- We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
- We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
- We prize innovation and seek intelligent solutions using leading-edge technology.
- Bachelor s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
- At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor s degree or equivalent. At least 6 years of related experience with a master s degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Strong SAS data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong QC / validation skills.
- Good ad-hoc reporting skills.
- Proficiency in Efficacy analysis.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.
- Submissions experience utilizing define.xml and other submission documents.
- Experience supporting immunology, respiratory or oncology studies would be a plus.
- Excellent analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
How you will contribute:
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
- Performing lead duties when called upon
- Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change
Employment Type: Full Time, Permanent
Read full job description
What people at Cytel Statistical Software & Services are saying
Senior Statistical Programmer salary at Cytel Statistical Software & Services
reported by
12
employees
with 3-7
years exp.
₹10
L/yr - ₹25
L/yr
16%
less
than the average Senior Statistical Programmer Salary in India
View more details
What Cytel Statistical Software & Services employees are saying about work life
based on 51 employees
Flexible timing
Monday to Friday
No travel
Day Shift
Cytel Statistical Software & Services Benefits
View more benefits
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