Jobs

Interviews
Job Alerts
Tools

Upskill and Grow with AI

Mock Interview Practice interviews in realistic simulations

Coding Practice Improve your coding skills with challenges

Certification Earn certifications to validate your skills

AI Learning Get trained with AI expert sessions

Career Path AI insights for smarter career decisions

AI Job Match Score AI-Powered Job Match Against Your Resume and Optimize Your Resume

Career Tools and Resources

Resume Builder Build Professional Resume with Ease

ATS Friendliness Check Check Resume Friendliness for Applicant Tracking Systems

Auto Apply Apply to hundreds of jobs on any platform effortlessly

Co-Pilot (Chrome Extension) Your AI Assistant for Seamless Browsing Efficiency

Interview Questions Streamline interviews with ready-to-use questions

Salaries Discover market-driven salary insights across skillsets and geographies

Companies Explore leading companies actively hiring talent
For Employers

Home

Jobs

Home
>
Jobs in Bengaluru
>
Sitero
>
Lead Statistical Programmer

Lead Statistical Programmer

Sitero

8 - 13 years

9 - 13 Lacs

Bengaluru

Posted:11 hours ago| Platform:

Apply

Skills Required

Graphics Computer science Manager Quality Assurance Process improvement Pharma Healthcare Clinical research Operations SQL Clinical data management

Work Mode

Work from Office

Job Type

Full Time

Job Description

Company Overview

Sitero is a leading organization specializing in clinical research and healthcare solutions. We are dedicated to advancing medical research and improving patient outcomes through innovative technologies and services. As we continue to grow, we are seeking a highly motivated and detail-oriented Lead Statistical Programmer to join our team and contribute to our mission.

Position Overview

The Lead Statistical Programmer will bring statistical programming and clinical expertise to the creation of SDTM and AdaM domains, as well as tabulations, graphics and listings derived from clinical trial data. Responsibilities include programming Data Management Listings in accordance with sponsor requirements, preparing, documenting and testing necessary programs and ensuring that programming code adheres to regulatory and company standards. The role also involves performing quality assurance on work done by others, supporting production activities and assisting in training new employees.

Primary Responsibilities

Provides data to clients (internal and external) in functional format by:

Creating and executing SAS edit check programs
Validating edit check programs using standard validation practices and processes
Developing SAS programs that convert data from EDC to protocol-specific SAS datasets in accordance with customer specifications
Assist with the creation of SAS-related project programming and validation documentation
Assist with the creation of SAS macro and format libraries
Ensures the quality of our clients data and data export by
Reviewing and approving User Requirement Specifications (URS), Clinical Data Management (CDM) conventions, and working procedure documents
Developing and implementing new CDM systems and enhancements to current CDM systems
Understand, create, and communicate information about creating CDISC-compliant datasets
Create documentation related to the generation of customer specific SAS datasets
Maintain the SAS environment by providing assistance in SAS installation, updates, and maintenance
Assist the Study Quality Representative in the testing of protocol specific SAS conversion programs

Ensures project timelines as they relate to Clinical Data Management operations by

Assessing and assigning target dates for project timelines in conjunction with manager
Adhering to target dates for project timelines
Communicating any changes in target date to appropriate personnel including
Project Manager Keeping department head informed of current issues
Maintains departmental productivity and identifies opportunities for greater departmental efficiencies and quality by:
Coordinating activities of the Clinical Programming department with related activities of other departments (operations programming, study QA, PM and DM) to ensure efficiency
Evaluating current procedures and work instructions for accomplishing department objectives in order to develop and implement improved procedures
Assisting the training department with the development and maintenance of Clinical Programming training materials

Secondary Responsibilities

Contributes to team effort by

Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned and deemed necessary

Maintains Technical Knowledge by

Attending and participating in applicable company sponsored training

Maintains Quality Service and Departmental Standards by

Reading, understanding and adhering to organizational Standard Operating Procedures ( SOP ) Assisting in establishing and enforcing departmental standards Reviewing and providing recommendations to management on operational procedures, and participating in process improvement initiatives

Qualifications

Education

Bachelor s degree in computer science, design or related field required
Educational background in human-computer interaction, usability, user-centered design, user experience, information design, applied psychology, cognitive science, human factors, informatics, computer science, or other design/applied science fields is a plus.

Experience

8+ Years of experience, SAS programming experience in pharmaceutical related industry - Required
5+ Years of experience, Experience working with CDISC, SQL, and Relational Databases - Required
3+ Years of experience, Understanding of database organization and how to extract data to generate listings and reports- Required

Additional skill set

Ability to work in group setting and independently; ability to adjust to changing priorities
Excellent attention to detail and orientation toward meticulous work
Strong interpersonal and communication skills, both verbal and written
Strong documentation and organizational skills
Ability to project and maintain a professional and positive attitude

Working conditions

Travel: 5-20%

Lifting: 0-25 lbs

Other: Computer work for long periods of time

THIS POSITION DESCRIPTION SHOULD NOT BE DEEMED ALL INCLUSIVE. ADDITIONAL REQUIREMENTS AND EXPECTATIONS MAY BE ASSIGNED. AT ALL TIMES, EMPLOYEES ARE EXPECTED TO ADHERE TO COMPANY POLICIES AND COMPANY SOPS.

More Jobs at Sitero

Assistant Manager - FP&A

Bengaluru

3 - 5 yrs

INR 20 - 25 Lacs

Senior Software Engineer

Bengaluru

5 - 8 yrs

INR 18 - 20 Lacs

Clinical Data Associate - I

Bengaluru

1.0 - 3.0 yrs

INR 2 - 6 Lacs

Automation Engineer

Bengaluru

3.0 - 5.0 yrs

INR 16 - 20 Lacs

Validation Analyst

Bengaluru

2.0 - 3.0 yrs

INR 4 - 5 Lacs

Mock Interview

Practice Video Interview with JobPe AI

Start Graphics Interview Now

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

Sitero

Design Services

Tech City

50-100 Employees

6 Jobs

Key People

John Doe

CEO
Jane Smith

CTO
Richard Roe

CFO

Login to

Please Verify Your Phone or Email

Confirm Action

Search

Profile

Upskill and Grow with AI

Lead Statistical Programmer