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Lambda Therapeutic Research

Technical Officer - SAS Programming - CT

Ahmedabad · Executive

Good timing - competition is buildingVerified listingPosted 16d ago

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Skills required

9 listed
Clinical ResearchClinical TrialsResource ManagementSAS/BaseSAS (Software)Phase (Waves)BiostatisticsAutomated Dynamic Analysis Of Mechanical Systems (ADAM)+1 more
Clinical ResearchClinical TrialsResource ManagementSAS/BaseSAS (Software)

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Job description

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 (Late Phase)
Reporting To Manager Biostatistics / Sr. SAS Programmer
Department Biostatistics & Programming
Location Ahmedabad
Overall Purpose SAS Programming for late phase trials

KEY DELIVERABLES

▪ SAS programming for Tables, Listings & Plots for early & late phase clinical trials

▪ Perform programmatical QC for SAS deliverables (like datasets & TLGs)

▪ Generation of Datasets (SDTM & ADaM) for clinical trials  ▪ Creation of CDISC documentation (like define.xml, csdrg & adrg, aCRF etc.)

▪ Provide inputs in SAP from Programming notes, Process and Mock shells

▪ Team overview, Resource management – training & quality improvisation steps

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)

▪ SAS programming experience of 3+ yrs in pharma / CRO setup

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Applicants who checked fit first are 3.1× more likely to hear back

Your match scoreFree · sign in
86Overall
64Skills
97Experience

Your score for this role already exists

ASAI compared this JD against 41 signals - skills, seniority, domain, stack overlap etc. Add a resume and it unlocks in about 30 seconds.

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Free · no signup

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Why people use ASAI

Someone shared one job with you. ASAI keeps finding the rest.

  • Scored, not searched. Every role ranked against your actual profile.

  • Alerts as often as hourly. Reach new roles while the pile is still small.

  • Skill gaps, spelled out. See exactly which requirements you don't meet yet.

  • Verified jobs, only. Say no to ghost jobs. Your time deserves respect.

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