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    Research Nurse

    Veeda Clinical Research Limited
    GNM / B.Sc Nursing years
    Not Disclosed
    Ahmedabad
    1 June 25, 2024
    Job Description
    Job Type: Full Time Education: GNM / B.Sc Nursing Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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

    Job Description: Research Nurse

    Company: Veeda Clinical Research Limited
    Location: Ahmedabad, India
    Position: Research Nurse
    Experience: 2-5 Years
    Qualification: GNM / B.Sc Nursing

    About Veeda Clinical Research Limited

    Veeda Clinical Research Limited is a leading global clinical research organization headquartered in Ahmedabad, India. We are dedicated to providing high-quality clinical research services to the pharmaceutical, biotechnology, and medical device industries. Our mission is to deliver excellence in clinical trials with a commitment to scientific integrity, regulatory compliance, and the highest ethical standards.

    Job Summary

    As a Research Nurse at Veeda Clinical Research Limited, you will play a crucial role in the clinical research process. You will be responsible for the coordination and conduct of clinical trials, ensuring that they are performed according to regulatory requirements and study protocols. You will work closely with clinical research coordinators, investigators, and other healthcare professionals to provide quality care to study participants and contribute to the advancement of medical research.

    Key Responsibilities

    • Patient Care and Management:

      • Recruit, screen, and enroll study participants according to study protocols and inclusion/exclusion criteria.
      • Provide nursing care to study participants, including administering medications, performing procedures, and monitoring vital signs.
      • Educate participants about study protocols, procedures, and potential side effects.

    • Study Coordination:

      • Coordinate and schedule study visits and procedures, ensuring compliance with study timelines and protocols.
      • Assist in obtaining informed consent from study participants and ensure that consent forms are properly documented.

    • Data Collection and Documentation:

      • Collect and record accurate and timely data related to study visits, procedures, and outcomes.
      • Maintain detailed and organized records of study activities, participant interactions, and adverse events.

    • Compliance and Quality Assurance:

      • Ensure that all study activities adhere to Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements.
      • Participate in internal and external audits and inspections, providing necessary documentation and support.

    • Collaboration and Communication:

      • Work closely with clinical research coordinators, investigators, and other healthcare professionals to ensure seamless study conduct.
      • Communicate effectively with study participants, addressing their questions and concerns promptly.

    • Training and Education:

      • Provide training and support to other nursing staff involved in clinical research activities.
      • Stay updated with the latest developments in clinical research and nursing practices through continuous education and professional development.

    Qualifications and Skills

    • Educational Background:

      • General Nursing and Midwifery (GNM) or Bachelor of Science in Nursing (B.Sc Nursing).

    • Experience:

      • 2-5 years of experience in clinical research, clinical trials, or patient care within a healthcare or research setting.

    • Technical Skills:

      • Proficiency in using electronic medical records (EMR) and clinical trial management systems (CTMS).
      • Strong understanding of clinical research protocols, GCP, and regulatory requirements.

    • Clinical Skills:

      • Excellent clinical and nursing skills, including patient assessment, phlebotomy, and medication administration.
      • Ability to perform clinical procedures and manage study-related emergencies effectively.

    • Organizational Skills:

      • Strong organizational and time-management skills.
      • Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.

    • Communication Skills:

      • Excellent written and verbal communication skills.
      • Ability to effectively interact with study participants, clinical staff, and other stakeholders.

    • Interpersonal Skills:

      • Compassionate and empathetic approach to patient care.
      • Strong interpersonal skills and ability to work effectively as part of a multidisciplinary team.

    What We Offer

    • Competitive salary and benefits package.
    • Opportunities for professional growth and development.
    • A supportive and collaborative work environment.
    • The chance to contribute to cutting-edge clinical research and improve patient outcomes.

    How to Apply

    Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience and qualifications to careers@veedacr.com with the subject line "Application for Research Nurse."

    Join Veeda Clinical Research Limited and be part of a team that is committed to advancing medical science and improving patient outcomes through high-quality clinical research.

    Note: This job description is intended to provide a general overview of the position and may include other responsibilities and qualifications as required by Veeda Clinical Research Limited.

     

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