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    Assistant Clinical Research

    Fortis
    0-3 years
    Not Disclosed
    Bangalore
    10 March 15, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm Skills: Causality Assessment, Communication Skills, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job description

    Fortis Healthcare Ltd is looking for Assistant Clinical Research to join our dynamic team and embark on a rewarding career journey

    • Assisting in Study Design: Collaborating with principal investigators (PIs) and senior researchers in designing clinical research studies, including protocol development, sample size calculation, and study endpoints.
    • Participant Recruitment: Assisting in the identification and recruitment of eligible participants for clinical trials, including obtaining informed consent and ensuring adherence to study protocols.
    • Data Collection and Management: Collecting and organizing research data according to study protocols, including patient demographics, medical histories, and study-specific assessments. This may involve utilizing electronic data capture systems and maintaining accurate and up-to-date records.
    • Study Coordination: Coordinating study activities and timelines, scheduling participant visits, coordinating study procedures (e.g., laboratory tests, imaging studies), and ensuring compliance with regulatory requirements.
    • Data Analysis: Assisting in the analysis of research data, including statistical analysis and interpretation of study findings. This may involve using statistical software such as SPSS or SAS.
    • Documentation and Reporting: Assisting in the preparation of study-related documentation, including research protocols, informed consent forms, and regulatory submissions. Additionally, helping in the preparation of study reports, abstracts, and manuscripts for publication.
    • Quality Assurance and Regulatory Compliance: Ensuring compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and institutional policies throughout the conduct of the study. This includes maintaining study documentation, conducting internal audits, and participating in regulatory inspections as needed.
    • Communication and Collaboration: Collaborating with interdisciplinary teams, including physicians, nurses, laboratory personnel, and statisticians, to ensure the smooth conduct of clinical research studies. Additionally, communicating study progress and findings to stakeholders such as investigators, sponsors, and regulatory agencies.
    • Training and Education: Participating in ongoing training and educational activities related to clinical research, including protocol-specific training, GCP training, and professional development opportunities.
    • Adherence to Ethical Standards: Upholding ethical standards in the conduct of clinical research, including protecting the rights and welfare of research participants and maintaining confidentiality of study data.

    Role: Clinical research Scientist

    Industry Type: Medical Services / Hospital

    Department: Research & Development

    Employment Type: Full Time, Permanent

    Role Category: Pharmaceutical & Biotechnology

    Education

    UG: Any Graduate

    PG: Any Postgraduate

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