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Study Nurse

Navitas Lifesciences
Navitas lifesciences
0-2 years
Not Disclosed
Manipal, Remote
10 April 21, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Title: Study Nurse

Department: Clinical Research / BA/BE Unit

Experience Required: 0–2 Years

Qualification: Nursing Council Registration Required


Role Overview

The Study Nurse is responsible for supporting clinical trial activities, including patient care, sample collection, documentation, and ensuring compliance with study protocols and SOPs. The role involves working closely with clinical teams to ensure smooth execution of studies.


Key Responsibilities

1. Patient Care & Clinical Procedures

  • Monitor and record vital signs as per SOPs and study protocols

  • Perform IV cannulation and blood sample collection during screening and study phases

  • Administer investigational products as per protocol

  • Assist in the management and reporting of adverse events

2. Sample & Laboratory Management

  • Label vacutainers and cryovials accurately

  • Verify sample labels for correctness and compliance

  • Segregate and handle biological samples as per protocol

3. Ward & Equipment Management

  • Manage BA/BE and ICU wards efficiently

  • Maintain ICU instruments and associated logbooks

  • Record temperature and humidity of wards and sample collection areas

4. Inventory & Emergency Preparedness

  • Maintain stock of emergency medicines and required materials

  • Update emergency medicine logbooks and relevant documentation

  • Ensure availability of supplies for phlebotomy and medical procedures

5. Compliance & Documentation

  • Ensure all study procedures follow SOPs and protocol requirements

  • Maintain accurate documentation including CRFs and logbooks

  • Ensure proper biomedical waste disposal as per SOP

6. Screening & Volunteer Management

  • Support volunteer screening and registration processes

  • Measure and record BMI during screening

  • Assist in compiling screening and study reports

  • Enter lab values and maintain study records

7. Administrative Support

  • Update training records for contract staff

  • Assist in study-related documentation and reporting activities


Required Skills & Competencies

  • Basic clinical and nursing skills

  • Knowledge of clinical trial procedures (preferred)

  • Good communication and interpersonal skills

  • Attention to detail and documentation accuracy


Technical Skills

  • Basic computer literacy for data entry and documentation


Preferred Experience

  • 0–2 years of nursing or clinical research experience

  • Registered with Nursing Council


Personal Attributes

  • Responsible and detail-oriented

  • Ability to work in a team and follow protocols strictly

  • Willingness to work in a clinical research environment

  • Good organizational and multitasking abilities