Lambda Hiring Technical Officers - CDM & SAS Programming
Are you seeking Lambda Therapeutic Research Careers or a Clinical Data Management Job in Ahmedabad? Global clinical research organization (CRO) Lambda Therapeutic Research Ltd. has announced multiple openings for Technical Officer – Clinical Data Management (CDM) and Technical Officer – SAS Programming.
These clinical trials data validation and biostatistics database programming vacancies are based at the Ahmedabad office. The roles are open to graduates and postgraduates holding degrees in Pharmacy, general Sciences, BHMS, BAMS, BDS, or Statistics (B.Pharm/M.Pharm/B.Sc/M.Sc). Candidates with 0 to 3 years of experience in eCRF design, data query management, or clinical SAS programming will find these positions highly suitable. Selected technical officers will design data validation rules, program statistical analysis listings, and check CDISC compliance. To write a resume detailing your database designs, SAS macros, or edit check milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Position & Requisition | Details |
|---|---|
| Technical Officer – Clinical Data Management (Early Phase) • Req ID: 1589 |
• Experience: 0-3 Years (Freshers Eligible) • Qualification: B.Pharm, B.Sc. • Focus: eSource CRF design, edit checks, testing for BA/BE studies |
| Technical Officer – SAS Programming (Clinical Trials) • Req ID: 1590 |
• Experience: 0-3 Years (Clinical SAS experience preferred) • Qualification: Postgraduate in Pharmacy, Statistics, or Science • Certification: SAS Base or Advanced Certification is MANDATORY • Focus: TLFs development, SDTM/ADaM generation, CDISC docs |
| Technical Officer – Clinical Data Management (Late Phase) • Req ID: 1588 |
• Experience: 0-3 Years (Freshers Eligible) • Qualification: M.Pharm, M.Sc. (Life Sciences), BHMS, BAMS, BDMS / BDS • Focus: eCRF design/testing, clinical data validation, medical coding, query logs |
| Expected CTC | ₹3,50,000 – ₹7,00,000 per annum (depending on qualifications and SAS certification) |
💼 Key Responsibilities
1. Technical Officer – CDM (Early Phase):
- eSource CRF Design: Design and test eSource CRFs for early-phase BA/BE and PK studies.
- Validation Logic: Develop edit checks and eCRF validation rules.
- Documentation Curation: Prepare and verify detailed eCRF guidelines.
- Testing Activities: Perform user acceptance testing (UAT) on study databases.
2. Technical Officer – SAS Programming (Clinical Trials):
- TLFs Development: Develop SAS programs for Tables, Listings, and Figures (TLFs) according to SAPs.
- CDISC Mapping: Generate, review, and validate SDTM and ADaM datasets.
- Quality Control: Perform programming quality checks (QC) and double-programming validations.
- Regulatory Docs: Create CDISC documentation including Define.xml, ADRG, CSDRG, and aCRFs.
3. Technical Officer – CDM (Late Phase):
- Database Validation: Design eCRFs and execute data validation plans for late-phase trials.
- Query Management: Log, track, and resolve data queries with investigative sites.
- Medical Coding: Code clinical parameters using medical dictionaries (MedDRA, WHODrug).
- Trial Close-out: Support database lock activities and external data reconciliations.
To learn how clinical data managers and clinical SAS programmers salaries compare to conventional pharmacovigilance drug safety associate and clinical monitoring roles, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- CDM Roles: B.Pharm or B.Sc (for Early Phase); M.Pharm, M.Sc (Life Sciences), or BHMS/BAMS/BDS (for Late Phase). Freshers are eligible to apply.
- SAS Programming: Master's degree in Pharmacy, Statistics, or general Sciences. SAS Base or Advanced certification is mandatory.
- Process Knowledge: Basic understanding of Clinical Data Management (CDM) standards, CDISC data guidelines, and the clinical research lifecycle.
- Communication: Strong written and verbal English communication to write documentation and query site coordinators.
For pharmacy and statistics graduates evaluating clinical database programming compared to conventional laboratory quality control or chemical formulation careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Lambda Therapeutic Research?
- Work inside a premier global CRO operating across India, Canada, US, and Europe.
- Obtain robust technical exposure across both early-phase BA/BE and late-phase global clinical trials.
- Enhance statistical analysis capabilities under experienced biostatisticians and SAS developers.
- Modern offices located in Gota, Ahmedabad, Gujarat.
To review your basic knowledge of patient registries, clinical data checks, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Operations vs Healthcare IT
Lambda Technical Officers design eCRFs, write SAS validation macros, and code medical histories, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Lambda Candidates
- Highlight SAS Certification: State your SAS credentials (e.g. Base SAS 9.4 Certified) clearly in the profile header.
- Quantify eCRF Validation: Mention database tools (Medidata Rave, Oracle Clinical) you have worked on.
- List Medical Coding: Detail any academic assignments coding clinical terms with MedDRA.
💬 Lambda CDM & SAS Interview Questions
- Q1. What is the difference between early phase and late phase clinical data management?
Answer Guidance: Early phase CDM (Phase I/BABE) deals with smaller patient cohorts, fast-paced timelines, and focuses heavily on PK/PD parameters and eSource data. Late phase CDM (Phase II-IV) involves large multi-site patient cohorts, extensive query logs, medical coding, and external data reconciliations. - Q2. Why are SDTM and ADaM datasets generated in clinical SAS programming?
Answer Guidance: SDTM (Study Data Tabulation Model) standardizes raw clinical trial data for submission. ADaM (Analysis Data Model) formats data specifically to support statistical analysis and TLFs, ensuring traceability. - Q3. Explain the term 'User Acceptance Testing (UAT)' in database setup.
Answer Guidance: UAT is the process where data managers test the configured electronic database using mock patient test data to verify that all screens, edit checks, and validation rules trigger correctly before the database is locked for live entry.
📄 Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Clinical Research, CDM, or SAS programming roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Lambda's official careers board. Click the links below to apply:
Apply for CDM (Early Phase) – Req ID: 1589 Apply for SAS Programming – Req ID: 1590 Apply for CDM (Late Phase) – Req ID: 1588❓ Frequently Asked Questions
Q. Is the SAS programming role open to freshers without certification?
No, a Base SAS or Advanced SAS certification is mandatory for the Technical Officer – SAS Programming position.
Q. What qualifications are required for the CDM Late Phase position?
Recruiters require an M.Pharm, M.Sc (Life Sciences), BHMS, BAMS, or BDS/BDMS degree for the Late Phase CDM role.
Q. Where are these Lambda Therapeutic Research positions based?
All three Technical Officer positions are full-time, office-based roles located at Lambda's corporate headquarters in Ahmedabad, Gujarat, India.
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