Statistical Programmer

As a Statistical programmer (all level) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working Location: India, Home-based

We are the global biostatistics team dedicated to late phase research, working on (but not limited to) peri and post approval research, post authorization safety studies, observational and non interventional studies, patient reported outcomes as well as analyses for abstracts, papers and manuscripts.

As a Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.

You Will Have Strong Demonstrable Experience In

• Create and Validate Safety and Efficacy Analysis Datasets in adherence with CDISC and client specific standards and maintain quality and accuracy.
• Create and Validate Safety and Efficacy Tables, Listings and Figures with high quality and accuracy.
• Create Study specific or general macros and finalize programming specifications/mock-ups.
• Adhere to programming specifications and study specific requirements, including completion and filing of required documentation.
• Plan and organize workload to ensure effective time management and adherence to project specific timelines.
• Proactively communicate and work effectively with the biostatistics team including remote teams and with senior programming, management and sponsor personnel to achieve study goals.
• Strong working knowledge of statistical concepts and its application in SAS.
• Demonstrate a constructive and flexible approach to project delivery, including problem solving, handling changing priorities and meeting study timelines.
• Learn, share and apply new techniques and technologies to increase efficiency and to implement industry trend solutions (e.g., SDTM, ADaM).
• Strong working knowledge of data structures (e.g., CDISC SDTM, ADaM), software development lifecycle and their implementation.
• Strong knowledge of the development, debug and use of standard programs and macros.
• Plan, organize and prioritize workload to ensure effective time management and adherence to project specific timelines.
• Participate in the review and approval of programming procedures and techniques.

#LI-remote

#LI-SO1

We Are Looking For

• Minimum Life Science/Pharma/Statistics /Software Engineering related degree or equivalent with 4+ years’ work experience in a SDTM, ADAM & TLF programming.
• 2 years of experience in R programming.
• Create and Validate Safety and Efficacy Tables, Listings and Figures with high quality and accuracy.
• Experience in creation of ADaM Datasets for Safety and efficacy domains.
• Very strong SAS programming skills required in SAS/Base, PROC SQL,SAS/Stat, SAS Macros and SAS/Graph (Base and Advance SAS).

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.