Technical Officer

ORGANISATIONAL OVERVIEW

We, Lambda Therapeutic Research Limited are a leading global Clinical Research
Organization (CRO) headquartered in Ahmedabad - India, with facilities and operations in Mehsana (India),
Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA) and Fargo (USA). Over 1500 employees are
working across the globe in these facilities.

Lambda offers Full-spectrum clinical trial solutions empowered by more than 20 years of service to the
biopharmaceutical and generic industry. At Lambda, our gamut of services under the clinical research domain
are executed with comprehensive efforts, to deliver positive results. Led by a management team of highly
qualified & experienced industry leaders, we apply innovative technologies, therapeutic expertise, and a
commitment to quality to help clients develop products safely, effectively, and quickly.

Delivering the best accomplished by hiring the best. Employees are the pillars that hold up every quality promise
that we make. That is why, we at Lambda are always looking for qualified and energetic individuals, with a desire
for excellence, to join our team.

JOB DETAILS

Job Role SAS Programmer Reporting To Head of Department / Project Head Department Clinical Data Management and Bio Statistics & Programming Location Ahmedabad Overall Purpose To be able to perform SAS Programming as per clinical study requiremen

KEY DELIVERABLES

CDISC SAS programming for early phase (BABE) & late phase (CT) projects Generation of Datasets (SDTM & ADaM) for clinical trials

Creation of CDISC documentation (like define.xml, csdrg & adrg, aCRF etc.)

Perform programmatical QC for SAS deliverables using Pinnacle Validator s/w

Review of eCRF annotation and coordinate with CDM & Clinic team for study data listings

Team overview, Resource management - training & quality improvisation steps

Overall Project Management for CDISC SAS deliverables & Timelines

ALLIED RESPONSIBILITIES

Any other responsibilities as assigned by the Head of the Department

EXPERIENCE

Should have Worked in SAS Programmer for 1 year in Clinical Research/Life Science domain.

EDUCATIONAL QUALIFICATION

SAS Base or Advanced Certification - mandatory requirements

Post-graduate (Science, Statistics or Pharmacy)

Good fluency in verbal & written communications (English & Hindi)

CDISC SAS programming experience of 2+ yrs in pharma / CRO setup

COMPETENCIES