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    Safety Science Coordinator Ii

    Fortrea
    1-3 years years
    Preffered by Company
    20 May 28, 2024
    Job Description
    Job Type: Full Time Education: BSC, MSC, B Pharma, M Pharma, Pharma D Skills: Causality Assessment, Communication Skills, CPC Certified, ICD-10 CM, CPT, HCPCS Coding, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Safety Science Coordinator II

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    Location: Pune, India

    Employment Type: Full Time

    Date Posted: Yesterday

    Job Requisition ID: 2421005

    Company Overview: Fortrea is a leading global Contract Research Organization (CRO) committed to advancing clinical development with scientific rigor. We serve pharmaceutical, biotechnology, and medical device companies by offering comprehensive clinical development, patient access, and technology solutions across over 20 therapeutic areas. With more than 19,000 employees in over 90 countries, our mission is to transform drug and device development worldwide.

    Job Description:

    • Report Handling: Receive and identify suspected ADR/ADE reports from various sources including mail, telephone, fax, email, or direct reports from clients or employees.
    • Data Verification and Record Management: Perform duplicate checks, verify important dates, and maintain records in compliance with client requirements.
    • Case Management: Acknowledge receipt of reports through email, fax, phone, or mail. Create new case entries in the Safety database as per client SOPs/WI for valid cases.
    • Documentation and Data Reconciliation: Ensure thorough documentation and perform data reconciliation from multiple sources including literature searches and reviews.
    • Medical Coding and Data Entry: Complete data entry and medical coding of all available data in the relevant safety database.
    • Follow-Up Initiatives: Initiate follow-up with reporters as per client SOPs/WI.
    • Narrative Compilation: Compile case narratives following Client Narrative Composition Guidelines.
    • Safety Report Review: Conduct reviews of safety reports to ensure accurate data entry.

    Join Our Team: Fortrea is looking for motivated problem-solvers and creative thinkers who are passionate about overcoming barriers in clinical trials. We are dedicated to revolutionizing the development process and delivering life-changing therapies swiftly to those in need. We offer a collaborative workspace that nurtures personal growth and enables you to make a significant global impact. For more information, please visit www.fortrea.com.

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