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    Zuventus Healthcare is Hiring: Freshers Pharma Clinical Research Associate | Apply Now

    Clinical Research Jobs at Zuventus Healthcare | Pharma Freshers Job | Apply Now

    Zuventus Healthcare Ltd. is offering one of the most promising Clinical Research Jobs for aspiring professionals and fresh graduates in Mumbai. This role is perfect for candidates looking to start their journey in the clinical research domain, especially those exploring Pharma Freshers Jobs that provide real exposure to protocol design, site monitoring, and regulatory documentation. With involvement across end-to-end clinical trial operations, this opportunity helps build a strong foundation for a long-term career in medical and clinical research.

    Job Details:

    • Job Title: Clinical Research Associate
    • Job Code: ZUV/CRA/1571100
    • Company: Zuventus Healthcare Ltd.
    • Location: ZHL HO Mumbai, Medical Services, Mumbai

    About The Company:

    Zuventus Healthcare Ltd. is a renowned name in the pharmaceutical industry, committed to improving healthcare by focusing on innovation, research, and development. Established with a mission to transform lives, we pride ourselves on producing high-quality pharmaceuticals and medical services that cater to the evolving needs of healthcare professionals and patients. Join us in our journey to bring exceptional health solutions to the world.

    Key Responsibilities in Clinical Research Jobs

    Financial:

    • Negotiating clinical trial budget with the CROs/Investigators.

    Operational:

    • Preparation and amendment of SOPs for clinical trial activities.
    • Clinical trial sites’ qualification and selection.
    • Tracking payments made to the CRO/Investigators/Ethics Committees.
    • Protocol Designing.
    • Case Report Form (CRF) Designing.
    • Preparation of dossier/documents for Regulatory submission.
    • Addressing DCG(I) queries.
    • Co-ordination with the CRO for timely completion of the clinical trial activities.
    • Protocol training of the study staff.
    • Monitoring and auditing clinical trial sites.
    • Coordinate with investigators for conduction of clinical trials.
    • Archiving study documentation and correspondence.
    • Source Data Verification: Verifying that data entered in the CRFs is consistent with source data.
    • Analyzing the clinical study data.
    • Preparing DCG(I) presentations.
    • Preparing Clinical study reports.
    • Preparing PSURs.
    • Preparing manuscripts for publication.
    • Reviewing the BA/BE protocols as per the regulatory requirements.

    Qualifications : Ideal for Pharma Freshers Jobs Applicants

    • Minimum Qualification: Master of Pharmacy (M.Pharm)
    • Education: Post Graduation
    • Skills: Clinical Research

    Link to Original Notification to Apply

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