Senior Clinical SAS Programming Operations Manager

3 days ago

Bengaluru, Karnataka, India beBeeOperations Full time ₹ 20,00,000 - ₹ 25,00,000
Operations Manager - Clinical SAS Programming">

We are seeking an experienced Operations Manager to oversee the day-to-day operations of our Clinical SAS Programming team. This role is critical in ensuring the timely delivery of programming outputs, optimizing team workflows, and supporting cross-functional collaboration across clinical development, biostatistics, and data management.

Key Responsibilities:

  • Manage timelines, resource allocation, and deliverables for clinical programming projects.
  • Track progress against milestones and proactively address risks or delays.
  • Ensure compliance with regulatory standards (CDISC, FDA, ICH-GCP).

Team Coordination:

  • Facilitate communication between programmers, statisticians, and data managers.
  • Support onboarding, training, and performance tracking of programming staff.
  • Promote a culture of accountability, collaboration, and continuous improvement.

Process & Quality Management:

  • Implement and maintain SOPs, workflows, and documentation standards.
  • Drive automation and efficiency improvements in programming operations.
  • Monitor quality metrics and ensure audit readiness.

Stakeholder Engagement:

  • Serve as the point of contact for operational updates to leadership and project teams.
  • Coordinate with global teams to align on priorities and resource needs.
  • Support strategic planning and capacity forecasting.

Qualifications:

  • Bachelor's or Master's degree in Life Sciences, Computer Science, or related field.
  • 7+ years of experience in clinical SAS programming, with 2+ years in a leadership or operations role.

Skills & Competencies:

  • Good understanding of clinical trial processes and CDISC standards (SDTM, ADaM).
  • Proficiency in project management tools (e.g., MS Project, Smartsheet, Jira).
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced environment.

Preferred Qualifications:

  • PMP or similar project management certification.
  • Experience working in a CRO or pharmaceutical company.
  • Familiarity with regulatory submission processes (e.g., eCTD, define.xml).

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