Lambda Hiring MD Pharmacology Specialists for Site Management Operations
Are you seeking Lambda Therapeutic Research Careers or a Clinical Operations Job in Ahmedabad? Leading global Contract Research Organization (CRO) Lambda Therapeutic Research has announced openings for Site Management Operations (SMO) specialists based at its Ahmedabad facility.
This medical monitoring and trial management role is ideal for MD Pharmacology or MD Clinical Pharmacology graduates with 0 to 3 years of experience. Candidates will handle site identification, medical feasibility reviews, safety query evaluations (AE/SAE), and regulatory compliance audits. To draft a resume detailing your clinical protocols and feasibility assessment highlights, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Lambda Therapeutic Research Limited |
| Job Role | Site Management Operations (SMO) |
| Hiring Location | Ahmedabad, Gujarat |
| Employment Type | Full-Time, Permanent |
| Experience Required | 0–3 Years (Fresh MDs Welcome) |
| Qualifications | MD Pharmacology / MD Clinical Pharmacology |
| Total Openings | 2 |
| Expected CTC | ₹16,00,000 – ₹20,00,000 per annum (Approx.) |
💼 Key Responsibilities
- Site Management & Feasibility: Oversee study site identification, feasibility assessments, site initiation, and close-out tasks.
- Medical Oversight: Act as the primary medical contact for clinical investigators, interpreting inclusion/exclusion criteria.
- Protocol Review: Review clinical protocols, informed consent documents, investigator brochures, and safety data.
- Pharmacovigilance & Safety: Conduct medical reviews of Adverse Events (AEs) and Serious Adverse Events (SAEs), performing causality assessments.
- Regulatory submissions: Coordinate with Ethics Committees (EC) and maintain the Trial Master File (TMF) archive.
- Oncology Trials: Provide specialized monitoring and endpoint support for complex oncology clinical trials.
To learn how clinical operations and medical monitoring salaries compare to conventional pharmacovigilance drug safety associate and clinical data programmer structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: MD in Pharmacology or MD in Clinical Pharmacology (mandatory).
- Experience: 0 to 3 years. Candidates with previous experience in clinical research, site operations, or medical monitoring will have an advantage.
- Guidelines Knowledge: Strong understanding of ICH-GCP, CDSCO, NDCTR, and international regulatory standards.
- Clinical Oversight: Ability to review safety profiles, laboratory results, and medical histories.
- Communication: Good written and verbal English communication, maintaining professional contact with investigators and sponsors.
For medical graduates comparing clinical operation structures to conventional formulation or laboratory research Tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Lambda Therapeutic Research?
- Work inside one of India’s leading CROs with a strong presence in global clinical trials.
- Diverse exposure across Phase I–IV clinical trials, safety management, and oncology research.
- Direct coordination with premium global sponsors and multinational clinical investigators.
- Excellent career acceleration inside corporate clinical medicine.
To review your basic knowledge of clinical trial assistant functions, data registries, and GCP principles before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Site Management Operations vs Healthcare IT
Site Management Operations professionals manage investigator sites, review patient eligibility, and oversee clinical safety documentation, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Lambda MD Candidates
- Highlight Medical Thesis: Emphasize your MD pharmacology research thesis, drug evaluations, or clinical trials training.
- Detail Regulatory Exposure: Mention if you have participated in ethics committee submissions, GCP trainings, or clinical trial feasibility reviews.
- Specify Therapeutic Areas: Explicitly detail any experience or projects in oncology, cardiovascular, or infectious disease pharmacology.
💬 Lambda Site Management Operations Interview Questions
- Q1. What are the key elements checked during a clinical trial feasibility assessment?
Answer Guidance: Feasibility assessments evaluate whether a site can successfully run a trial. Key factors include investigator qualifications, patient population access, diagnostic equipment availability, staff resources, storage conditions for the investigational product, and competing studies. - Q2. How is causality assessed for an Adverse Event (AE) in a clinical trial?
Answer Guidance: Causality is assessed by looking at the temporal relationship between drug administration and AE onset, checking if the AE resolves when the drug is stopped (dechallenge) or recurs if restarted (rechallenge), and evaluating alternative causes like underlying disease or concomitant medications. - Q3. Explain the function of an Ethics Committee (EC) in clinical research.
Answer Guidance: The primary role of an EC is to safeguard the rights, safety, and well-being of clinical trial participants. They review the clinical protocol, informed consent documents, and investigator qualifications to approve or reject the initiation of trials at specific sites.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Lambda's recruitment page on Naukri. Click the button below to apply:
Apply Online – Lambda Naukri Application Page❓ Frequently Asked Questions
Q. Which qualifications are accepted by Lambda for this SMO role?
Candidates must possess an MD in Pharmacology or an MD in Clinical Pharmacology to apply.
Q. Can fresh MD Pharmacology graduates apply for this opening?
Yes. This position is open to freshers as well as professionals with up to 3 years of clinical operations or monitoring experience.
Q. What is the work location?
This is a full-time, permanent position based onsite at Lambda Therapeutic Research's headquarters in Ahmedabad, Gujarat, India.
.png)
