Senior Statistical Programmer

Myraid; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Myraid is seeking a lead clinical trial SAS programmer for Phase II-IV studies. You will lead SAS programming efforts and ensure compliant CDISC SDTM/ADaM deliverables, including Define.xml and eCRT, while coordinating timelines across multi-disciplinary teams.

You will mentor junior staff, support therapeutic area studies (including oncology), and contribute to statistical deliverables with a strong CS/stats background.

Qualifications

• 5–9 yrs clinical/CRO experience.
• 5+ yrs in SAS programming.
• Experience with end-to-end SDTM/ADaM.
• Exposure to 2+ therapeutic areas including oncology.
• Strong background in statistics or CS.

Responsibilities

• Lead clinical trial SAS programming efforts for Phase II-IV.
• Create and validate CDISC SDTM, ADaM, TLFs, and regulatory deliverables (Define.xml, eCRT).
• Manage project timelines and deliverables.
• Mentor junior staff and support multi-disciplinary clinical study teams.

Skills

Clinical trials

CRO experience

Statistics background

Project mentoring

Tools

SAS

Job description

Lead clinical trial SAS programming (Phase II-IV). Create & validate CDISC SDTM, ADaM, TLFs, & regulatory deliverables (Define.xml, eCRT). Manage project timelines, mentor junior staff, & support multi-disciplinary clinical study teams.

Required Candidate profile

5–9 yrs clinical/CRO experience with 5+ yrs in SAS. Expertise in end-to-end SDTMs/ADaMs, TLFs, & 2+ therapeutic areas (including oncology). Strong background in statistics or CS.