Job Title: Senior Research Associate
Job Category: Clinical Research / Clinical Operations / Nursing
Job Type: Full-Time
Location: Ahmedabad, Gujarat, India
Req ID: 1305
CTC Range: INR 4,00,000 – 7,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization provides comprehensive end-to-end clinical research services to innovator, biotechnology, and generic pharmaceutical companies worldwide.
With a strong international footprint across India, the United States, Canada, Poland, and the United Kingdom, Lambda delivers regulatory-compliant, high-quality clinical trial execution aligned with global standards.
Role Overview
We are seeking a highly skilled Senior Research Associate with a nursing background to support clinical trial operations, subject care, and paramedical procedures within a controlled research environment. The ideal candidate will bring strong clinical expertise, ICU exposure, and hands-on experience in patient monitoring, emergency response, and phlebotomy within hospital or clinical research settings.
This role is critical in ensuring subject safety, protocol adherence, and high standards of clinical excellence in regulated research environments.
Key Responsibilities
Monitor and record vital signs including blood pressure, pulse rate, temperature, and ECG.
Collect blood samples and manage phlebotomy-related procedures as per protocol.
Perform nursing duties during subject screening and provide care across clinical units.
Assist in dosing activities, including medication administration as per study requirements.
Support ICU operations and handle emergency procedures, including RT insertion and Foley catheterization.
Assist in calibration and maintenance of medical equipment such as sphygmomanometers, thermometers, cardiac monitors, and ECG machines.
Ensure proper biomedical waste segregation and disposal in compliance with regulatory guidelines.
Maintain hygiene, cleanliness, and infection control standards across clinical areas.
Manage stock and inventory of clinical, paramedical, and phlebotomy supplies.
Act as a clinical custodian, assisting with subject meals, bedding, and overall well-being during study participation.
Required Experience
5 to 7 years of professional experience in clinical operations, hospital settings, or clinical research units.
Proven experience in ICU management, emergency handling, and advanced nursing procedures.
Strong hands-on experience in phlebotomy, ECG monitoring, and subject care.
Familiarity with GCP guidelines and clinical research compliance standards is preferred.
Ability to work in regulated environments with high documentation accuracy.
Educational Qualification
B.Sc. Nursing (mandatory).
Experienced nursing professionals seeking career advancement in clinical research and regulated trial environments are encouraged to apply through ThePharmaDaily.com for confidential consideration.
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