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Medical Writer I

3-5 years
Preferred by Comapny
10 Nov. 25, 2024
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences,A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine/Nursing is advantageous. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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 Purpose:

This role is responsible for managing both scheduled and unscheduled aggregate safety reports, including but not limited to Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Semi-Annual Safety Reports (SASRs), Drug Safety Reports (DSRs), Risk Management Plans (RMPs), and Clinical Study Report (CSR) narratives, among others. The role also includes preparing and submitting regulatory documents, performing signal detection, ensuring data consistency across reports, and collaborating with clients and stakeholders to maintain high-quality deliverables. Additionally, the role involves providing input for literature reviews and epidemiological studies related to safety evaluations.


Key Accountabilities:

  1. Aggregate Reports Management:

    • Prepare and update Periodic Safety Reports (PSURs), PBRERs, Safety Evaluation Reports (SERs), and other related documents.
    • Conduct literature reviews and apply epidemiological methods to support safety evaluations.
    • Generate Line Listings for submissions and resolve discrepancies.
  2. Clinical Study Report Narratives:

    • Create accurate and clear narratives for Clinical Study Reports based on clinical and safety database outputs, ensuring medical cohesiveness and client requirements.
    • Perform quality checks on drafted narratives.
  3. Signal Detection and Management:

    • Perform qualitative and quantitative signal detection analysis from multiple data sources.
    • Manage the end-to-end signal management process in collaboration with the safety science team, including signal tracking, assessment, and leading review meetings.
  4. General Responsibilities:

    • Stay informed on adverse event safety profiles, regulatory reporting obligations, and maintain awareness of global safety regulations.
    • Prepare for audits and inspections, and maintain high-quality deliverables in all areas of safety reporting.
    • Delegate tasks and mentor new team members as needed.
    • Serve as the primary point of contact with clients, addressing any issues or feedback promptly.
    • Assist in archiving source documents and related communication for compliance.

Skills:

  • Strong analytical and problem-solving skills.
  • Excellent verbal and written communication, organizational, and prioritization abilities.
  • Ability to work collaboratively in teams and manage multiple tasks effectively.
  • Knowledge of medical terminologies and regulatory pharmacovigilance practices.
  • Proficiency in MS Office, web-based applications, and familiarity with Windows operating systems.
  • Client-focused with the ability to manage projects and deadlines.

Education and Experience:

  • A university degree in Life Sciences/Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, etc.) is required.
  • A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine/Nursing is advantageous.
  • Previous experience in regulatory or pharmacovigilance-related fields is desirable.