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Hiring CRA, Business Development, Biostatistics & PK Roles
Lambda Therapeutic Research
Ahmedabad
0–5 Years
CRO
Clinical / SAS / PK
🏢 About Lambda CRO
Lambda Therapeutic Research is a globally recognized CRO audited by USFDA, EMA, and MHRA. The company specializes in clinical trials, bioequivalence studies, pharmacokinetics, and biostatistics.
1️⃣ Clinical Research Associate I (CRA I)
- Experience: ~5 Years
- Clinical data mining & trial tracking
- Work on clinicaltrials.gov & regulatory databases
Skills: Excel, Data Analysis, Clinical Research
Tip: Prepare regulatory & trial lifecycle questions
2️⃣ Executive – Business Development
- Experience: 3–5 Years
- Client acquisition & market research
- Proposal & CRM management
Skills: Communication, Sales, Pharma knowledge
Tip: Be ready for client scenario questions
3️⃣ Technical Officer – Biostatistics & Programming
- Experience: 1–4 Years
- SAP, TLFs & statistical analysis
- Work on SAS & clinical datasets
Skills: SAS, CDISC, Statistics
Tip: Practice SAS coding + TLF concepts
4️⃣ Technical Officer – PK Reviewer
- Experience: 1–3 Years
- PK/PD analysis & reporting
- BA/BE study review
Skills: Pharmacokinetics, Analysis
Tip: Revise PK parameters (Cmax, AUC)
💰 Salary Range
- CRA: ₹5 – ₹8 LPA
- BD: ₹5 – ₹9 LPA
- Biostatistics: ₹4 – ₹8 LPA
- PK: ₹3 – ₹6 LPA
🚀 Select Role & Apply Directly
🔍 Apply: Clinical Research Associate I (CRA I)
💼 Apply: Executive - Business Development
📊 Apply: Technical Officer - Biostatistics & Programming
🧪 Apply: Technical Officer - PK Reviewer
💡 Lambda CRO Professional Screening Compliance Guide:
Lambda's global research divisions execute applicant tracking parsing based on operational core keywords. Before final submission of your credentials on their portal setup, make sure your resume highlights specific professional milestones matching the division criteria:
Lambda's global research divisions execute applicant tracking parsing based on operational core keywords. Before final submission of your credentials on their portal setup, make sure your resume highlights specific professional milestones matching the division criteria:
- Clinical Monitoring (CRA): Focus on source data validation (SDV), investigational product tracking logs, trial site essential documents, and monitoring reports.
- Commercial Operations (BD): Emphasize response metrics for Requests for Proposals (RFPs), pharmaceutical client relationship frameworks, and service-level agreement targets.
- Biostatistics: Target programmatic execution of analysis datasets, validation of derivation specs, and generation of production tables, listings, and figures (TLFs).
- Pharmacokinetics (PK): Validate strong tracking of non-compartmental analysis (NCA) parameters, bioequivalence study data, and review of draft study validation reports.
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