Designation – Senior Statistical Programming
Location – Pune, Navi Mumbai, Bangalore, Hyderabad
About employer– Cytel
Job description:
Responsibilities
- Working under the direction of Team Lead / Project Manager, the senior statistical programmer conducts programming activities for trials, early phase projects, indications, or publications activities
- Lead at least one study team in terms of providing technical and domain related guidance
- May require to lead and manage a team of 2-4 members
- Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard
- Read and understand the program specifications document
- Prepare SAS analysis datasets, tables, listings, and figures as per specifications
- Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery
- Validate tables, listings, and figures as per client assignment specifications
- Co-ordinate with the client and the US team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
- Contribute in the organization’s recruitment process by identifying needs and the required skill set of resources, and conducting interviews to hire appropriate resources
- Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System
Qualification and Skills Required
- Bachelor or Master’s degree in Computer Science, Statistics or related Health Science field.
- Experience:
- A minimum of 4 – 5 years’ of SAS programming experience with clinical trial data
- Well conversant with regulatory requirements and drug development process
- Good understanding of the clinical trial domain and good SAS programming skills
- Ability to work independently
Interested people can apply for this job can mail their CV to [email protected] with subject as Senior Statistical Programming – Cytel – Bangalore
