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Pv Assistant Manager, Aggregate Report Writing

5+ years
Not Disclosed
10 Oct. 24, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Grow with Us!
Are you looking for a dynamic company that offers daily challenges and opportunities? Look no further—Pharmalex is your career destination! As one of the leading service providers in the pharmaceutical industry globally, Pharmalex specializes in all aspects of drug and medical device approvals, market development, and effective product maintenance.

Position: PV Assistant Manager, Aggregate Report Writing

Your Role

  • Safety Report Development:
    Lead the development, authorship, and tracking of Safety Reports (PSUR/RMP/ACOs) to ensure high-quality, regulatory-compliant documents. Manage logistics and distribution in a timely manner.

  • Operational Implementation:
    Implement operational tasks related to safety writing and oversee service performance.

  • Mentorship:
    Mentor team members, enabling them to work independently within established timelines, budgets, and quality standards.

  • Kick-off Meetings:
    Organize kick-off meetings and prepare PSURs and RMPs according to client SOPs, ensuring medical cohesiveness and safety concern characterization.

  • Document Collaboration:
    Collaborate with various teams to develop and author high-quality, compliant PSUR-PBRER, RMP, ACO, and DSUR documents.

  • Logistical Coordination:
    Manage all logistical aspects related to the timely development of safety reports, ensuring that content meets client and Health Authority requirements.

  • Regulatory Updates:
    Update the RMP in accordance with Health Authority requirements, ensuring alignment with other regulatory documents like the PSUR and CDS.

  • Consistency and Compliance:
    Ensure regulatory compliance and consistency of RMP/PSUR/ACO sections and annexes. Track feedback from Health Authorities and implement necessary changes.

  • Training Development:
    Develop and dispatch product-specific training materials for internal staff and third-party training.

  • Peer Review and Quality Control:
    Conduct peer reviews, populate QC checklists, and address comments from stakeholders.

  • Health Authority Responses:
    Prepare responses to Health Authority requests and formulate strategies for safety issues and integrated benefit-risk evaluations.

Your Profile

  • Experience:
    Minimum of 5 years in aggregate report authoring (Innovators).

  • Qualifications:
    B.Pharm, M.Pharm, BDS, or Pharm D.

How to Apply

If you are interested in this challenging opportunity at Pharmalex, we look forward to receiving your application. Please include your earliest possible starting date, any visa requirements, and salary expectations. Join us in shaping the future of pharmacovigilance.