Senior Clinical SAS Programmer

At Elanco (NYSE: ELAN) - it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals lives better makes life better - join our team today!

Your Role: Senior Clinical SAS Programmer

This position is expected to be highly influential in partnering with product development teams and third parties to develop data management strategies that result in on-target delivery of final databases. This position will closely collaborate with R&D functions including clinical development, internal study sites, biostatistics, regulatory affairs, and quality assurance to ensure data integrity, data quality, validation, and compliance

Your Responsibilities: -

• Proactively search for solutions.

• Work effectively and flexibly within and across all Elanco R&D teams and external collaborators to achieve overall Elanco R&D deliverables.

• Create a positive work environment that is aligned with companyobjectives.

• Provide and acceptchallengeto deliver innovative technical solutions and create an innovative culture.

• Create an engaging culture with a Play to Win mentality.

• Identifyandutilizemethods to deliver individualobjectivesin a high quality,timely, cost-effective manner.

• Demonstratehigh levelsof adaptability, flexibility, and learning agility

Key Technical Responsibilities

• Use SAS or other software to develop custom programmingreports helpingindata cleaning activities.

• Ensure that outputs meet quality standards and project requirements.

• Performvalidationprogramming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.

• Ensure adherence to clinical data collection policies and procedures and is expected to keep Elanco at the forefront of standards for the animal health industry

• Keep project team members informed of programming progress and issues requiringtheir attention.

• Confirm validation and compliance to all regulations (includingGxP) and guidelines the global data management systems and processutilizedto collect, manage, report, store and archive databasescontainingclinical data

• Be part of the regular connects with site lead and study team (Site/Study program leads).

• Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload.

• Prepare in advance for internal meetings, contribute ideas, anddemonstraterespect for opinions of others.

• Negotiate andestablishaccuratetime estimates for completion of study programming activities with internal team members.

• Assistin drafting regulatory submissions.

• Ensure scientific integrity and animal welfare in all activities.

• Create andmaintainstandard macros and applications to improve the efficiency of the department.

• Develop wider knowledge of SAS and other relevant programming languages and processeswithin theData Management, Biostatistics and Medical arenas.

• Contribute to the mentoring of other programmers, developing training courses, presenting training materials, providing feedback, or guiding new associates inprocess.

• Participate in internal/external audits and regulatory inspections asrequired.

• Engage in knowledgeshareactivities

What You Need to Succeed (minimum qualifications):

.BSc / MSc in related fields

.Minimum 10 years of relevant experience (some vaccine development experience will be a plus)

.Expertise in SAS programming with associated basic and advance certifications.

.Strong GxP knowledge, in particular GLP, GCP and GMP.

.Good written and verbal communication skills

What will give you a competitive edge (preferred qualifications):

.Clinical trial experience and/or clinical trial data experience

.Knowledge of electronic data capture systems

.Experience interacting with regulatory authorities and regulatory submissions

.Ability to communicate logically and technically. Deliver all communication with clarity, impact and passion tailored to the audience.

.Organizational planning skills, ability to manage competing priorities and flexibility to change.

.Commitment to quality.

.Ability to work independently or as part of a team.

High competency in Microsoft Office.

Additional Information:

• Travel:0%
• Location: India, Bangalore

Don't meet every single requirementStudies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our