Statistical Programmer
About the Job
The SAS Programmer will be responsible for providing SAS programming support for the Statistics and Data Management functions for all clinical trials and regulatory submissions. The candidate will work closely with Biostatisticians and Data Managers to create SAS programs for independently validating selected tables, listings, and figures and to assist with data cleaning and query generation. This position will also serve as a contact for programming activities being performed.
Key Activities
- Perform data manipulation techniques and advanced techniques (arrays, transpositions, complex merges, SQL, SDTM etc.) and generic macro use and development to enable listing, table, and graph generation.
- Involve in Statistical programming and validation of CDISC SDTM, Analysis Datasets (ADaM) and Tables, Listings, Graphs (TLG’S)
- Analyze information and develop innovative solutions to programming and data analysis challenges.
- Efficiently produce quality results under time constraints.
- Successfully coordinate multiple priorities.
- Based on experience, serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures.
- Assist internal project team in identifying project priorities and communicating such activities and associated timelines to departmental management
- Work independently to carry out assignments with occasional support from senior management.
- Ensure the efficiency, quality, and integrity of data reporting and project activities executed.
- Represent the department in client meetings/presentation and maintain a positive working relationship with sponsors, collaborating associate and vendor personnel.
- Actively adapt and adjust priorities to ensure timely and quality completion of assigned tasks.
- Contribute to on-going improvement of programming processes and methodology.
- Perform other related duties as required by the Department.
- Coach and advice junior programmers to identify problems and solutions
- Ability to adapt and adjust to changing priorities
- Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities, and deliverables.
- Ability to fulfill ad hoc requests and perform high level review on deliverables.
Required Skills/ Experience
- MSc in Biostatistics, Statistics, Computer Science, or related field.
- 2-7 years of experience, or an equivalent combination of education or experence to successfully perform the key responsibilities of the job
- Experience leading statistical programming activities in clinical research for 3 + years experienced candidates.
- SAS Certified Candidates preferred
- Good understanding of Clinical Trials and the various terminologies
- Experience leading statistical programming activities in clinical research
- Previous experience in pharmaceutical research or CRO setting
- Work within a team environment under extremely tight deadlines, and finish all TLGs ahead of schedule, despite severe data issues requiring multiple re-extractions and reruns
- Knowledge of one or more statistical sof tware packages (SAS® preferred) used to perform statistical analyses
- Knowledge of CDISC services and hands on experience in developing SDTM datasets.
- Good verbal and written communication
- Positive attitude and willingness to learn and contribute to a team setting
- Demonstrates ability to successfully lead a single project
About Genpro
Genpro is headquartered in Waltham, MA with offshore offices in India. We help our clients to
accelerate clinical research by applying AI, Machine Learning, NLP, Biostatistics, Medical Writing and Statistical Programming.
Genpro brings together an experienced team of statisticians, statistical programmers, data
managers, medical writers, and clinical data scientists. Our team of experts drives innovation and foresight to deliver simple solutions to most complex problems.
Our team includes some of the most experienced and innovative professionals in the clinical research segment. We are excited to tell you about the value that we have collectively created.
We are even more excited to drive success for you.
Experience
5 – 8 Years
Employment Type
Full-time
Work Location
Trivandrum / Permanently Remote
How to Apply
Subject: “Job Application: Statistical Programmer”
Send your application to the above-mentioned email address with your resume in PDF format.
Please include links to any of your works / git repositories for standing out.
