Senior Statistical Programmer - Bengaluru - Veramed

    Veramed
    Veramed Bengaluru

    6 days ago

    Default job background
    Description

    Principal SAS Programmer

    Location: Bangalore/Hyderabad/India Remote Opportunities

    We at Veramed pride ourselves on delivering exceptional statistics and programming consultancy services to our clients, while also providing an industry-leading work environment that fosters career growth and employee support.

    This role is for a hands-on SAS Programmer with strong attention to detail and a proven work ethic. As part of our statistical and programming team, you will provide programming support to various clients in the Veramed portfolio.

    You will have the opportunity to progress towards becoming a Lead Programmer at Veramed.

    Key Responsibilities:

    • Program and QC datasets and TFLs following specifications and good programming practice.
    • Develop dataset specifications that conform to CDISC data standards.
    • Attend and contribute to internal and client study team meetings.
    • Mentor less experienced members of the team.

    Daily Interactions:

    • Communicate directly with other study team members and client key contacts.
    • Share updates on ongoing work internally and at client meetings.
    • Collaborate with the internal Veramed team to deliver high-quality work on time.
    • Contribute programming expertise and wider industry knowledge as required.
    • Provide support and mentoring for more inexperienced members on the team.

    Opportunities for Growth:

    • Development into lead programmer or technical role.
    • Gaining experience across different therapeutic areas and phases.
    • Presenting at conferences.
    • Peer mentoring and/or line management.
    • Developing innovative solutions to aid study reporting.
    • Contributing to initiatives that consider employees, the environment, and local communities as part of our B Corp accreditation.

    What to Expect:

    • A warm and friendly working environment that supports your personal and professional growth.
    • A supportive management policy that provides tools for career development and success.
    • Exposure to a wide range of clients and projects, allowing you to diversify your workload and work closely with leading pharmaceutical companies.
    • The ability to own your role and develop your skills and experience.

    Desirable Experience:

    • Understanding of the clinical drug development process and relevant disease areas.
    • Awareness of industry and project standards as well as ICH guidelines.
    • Proficiency in using SAS or other statistical software (e.g., R) appropriate to the level of seniority.
    • A good understanding of CDISC data standards.
    • Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
    • Ability to work independently and as part of a team.
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