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0-2 years
Not Disclosed
10 Sept. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Study Nurse

Job Overview

We are seeking a Study Nurse to support clinical research activities, including patient care, sample collection, study procedures, and documentation in compliance with study protocols and SOPs. This role is essential for ensuring high-quality data collection and safe participant management.


Key Responsibilities

Clinical & Participant Care

  • Check and record vital signs as per SOP and study protocol.

  • Report and assist in the management of adverse events.

  • Perform IV cannulations and collect blood samples during study and screening.

  • Administer investigational products as per study protocol.

  • Conduct volunteer screening and registration, including checking BMI.

  • Ensure all study procedures are carried out in compliance with SOPs and protocols.

Sample & Laboratory Management

  • Label vacutainers and cryo vials; verify labels before processing.

  • Segregate samples and enter lab values into study databases.

  • Compile screening reports and study reports.

Ward & Emergency Management

  • Maintain and update stock of emergency medicines; complete related forms.

  • Manage BA/BE and ICU wards, including maintaining instruments and logbooks.

  • Record temperature and humidity of wards, sample collection areas, and ICU.

  • Ensure disposal of biohazard waste according to SOP.

  • Maintain adequate stock materials for phlebotomy and other medical activities.

Administrative & Documentation Tasks

  • Update contract staff training files.

  • Support screening and registration activities for clinical studies.

  • Ensure all documentation, including vital CRFs, logbooks, and study forms, is accurate and complete.


Required Qualifications & Experience

  • Experience: 0–2 years in a nursing role.

  • Registration: Registered with the Nursing Council.

  • Skills:

    • Good communication skills

    • Computer literate


Why Join

  • Contribute to clinical research and patient safety.

  • Gain exposure to BA/BE and ICU ward management and clinical trial procedures.

  • Work in a structured, protocol-driven environment supporting study success and high-quality data collection.