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    Safety Monitor Job in Clinical Research At Emmes Group | Pharma Apply Now

    Safety Monitor Job in Clinical Research At Emmes Group

    Emmes Group is hiring a Safety Monitor to support global clinical research projects through hands-on pharmacovigilance and safety monitoring activities. This Pharmacy Job role is ideal for life science, pharmacy, nursing, or clinical research professionals looking to build a career in drug safety, GVP, and clinical trial monitoring. Graduates seeking Pharmacy Jobs and want to start your career with Pharmacy Careers can apply now.

    Pharmacy Job Details

    • Job Title: Safety Monitor
    • Location: India (Remote / Bangalore)

    About the Company

    Emmes Group is a global clinical research organization with over 47 years of experience, known for its work with government agencies, public-private partnerships, and commercial biopharma. Emmes specializes in vaccines, infectious diseases, rare diseases, neuroscience, ophthalmology, and cell & gene therapy, with a strong patient-centric research approach. This Pharmacy Job role plays a significant role in the company.

    Educational Requirements

    • Bachelor’s degree in Pharmacology

    Key Responsibilities

    • Assist in safety monitoring activities in collaboration with Medical Monitors and project teams
    • Review and assess adverse events (AEs) and serious adverse events (SAEs)
    • Perform first-line evaluation of SAEs and prepare safety narratives
    • Support collection, assessment, monitoring, and reporting of safety data from clinical trials, RWE projects, spontaneous reports, and literature
    • Communication with investigator sites to obtain additional safety information when required is essential for this Pharmacy Job.
    • Coordinate timely submission of safety reports to regulatory authorities and sponsors
    • Maintain and reconcile SAE databases
    • Support DSMB, SRC, and Protocol Safety Review Team activities
    • Contribute to safety sections of protocols, safety management plans (SaMP), SOPs, and reports
    • Perform MedDRA and WHO Drug coding
    • Ensure compliance with GCP, GVP, and quality standards
    • Participate in audits, quality assurance activities, and process improvement initiatives

    Skills Required for this Pharmacy Job

    • Knowledge of pharmacovigilance and clinical trial safety monitoring
    • Understanding of GxP principles (GCP, GVP)
    • Strong clinical judgment and attention to detail
    • Ability to analyze and communicate safety data clearly
    • Excellent written and verbal communication skills
    • Team-oriented mindset with cross-functional collaboration ability
    • Graduates seeking Pharmacy Jobs and want to start your career with Pharmacy Careers can apply now.

    CLICK HERE TO APPLY ONLINE

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