Principal Statistical Programmers at SuperStaff

Manila, Metro Manila, Philippines -

Full Time

Start Date

Immediate

Expiry Date

09 May, 26

Salary

0.0

Posted On

08 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

SAS Programming, Statistical Programming, Oncology TA, Data Migration, CDISC Standards, Clinical Trial Data, Regulatory Requirements, Drug Development Process, Data Validation, Technical Guidance, Team Leadership, Client Coordination, Recruitment Process, Quality Management System, Graph Creation, Table Creation

Industry

Outsourcing/Offshoring

Description

We are looking for experience Statistical Programmers to work with one of our clients. Job Responsibilities Working under the direction of the Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities. Lead at least one study team in terms of providing technical and domain-related guidance. May required to lead and manage a team of 2-4 members Experience of working on Oncology TA is mandatory. 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 and transform datasets as per client assignment specifications. Validate tables, listings, and figures as per client assignment specifications. Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc. Contribute in the organization’s recruitment process by identifying needs and required skill sets 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 or the respective client(s) as applicable BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data. Well-conversed with regulatory requirements and drug development process. Good understanding of the Clinical trial domain and good SAS programming skills Ability to work independently. HMO with 1 free dependent upon hire Life Insurance 10% Night Differential 20 PTO credits annually VL and SL cash conversion Annual Performance-Based Merit Increases and Employee Recognition Great Company Culture Career Growth and Learnings Night Shift Work from Home Disclaimer: This job posting is for potential client opportunities and is intended for candidate pooling purposes only. By submitting your application, you are expressing interest in future positions with our clients. This does not guarantee immediate employment or an offer for a specific role

Responsibilities

The senior statistical programmer conducts programming activities for trials and leads study teams by providing technical and domain-related guidance. Responsibilities include preparing SAS analysis datasets, validating datasets, and coordinating with clients.