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Aggregate Report Specialist

5-8 years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

📌 Aggregate Report Specialist | Drug Safety Services - Mysore, Karnataka
📍 Location: Mysore, Karnataka, India
💼 Company: Sitero
🕒 Experience: 5+ years in Aggregate Report authoring

Role Overview

The Aggregate Report Specialist plays a critical role in reviewing and analyzing safety data, authoring, and reviewing reports for both pre-marketing and post-marketing safety assessments. This individual collaborates closely with project teams and external partners to ensure compliance with regulatory standards and submit high-quality reports. This role requires strong knowledge of pharmacovigilance regulations and drug safety practices.

Key Responsibilities

Safety Data Analysis: Analyze and interpret both non-clinical and clinical safety data for inclusion in aggregate reports.
Report Authoring & Review: Author and review PSURs, PBRERs, PADERs, Annual Reports, and other safety documents for regulatory submission.
Literature Search: Perform literature searches and present relevant articles for the preparation of aggregate reports.
Process Management: Manage trackers and reconcile safety data processes.
Subject Matter Expertise: Serve as a subject matter expert (SME), providing training and mentoring to junior staff.
Client Interaction: Collaborate with clients to resolve issues related to aggregate report submissions.
Regulatory Compliance: Ensure that reports comply with relevant regulatory requirements and timelines.

Qualifications

🎓 Education:

  • Degree in Life Science, Pharma, or a related field.

💼 Experience:

  • Minimum of 5 years of experience in authoring aggregate reports, with at least 3 years in quality review.

Desired Skills

  • 5-8 years of experience in aggregate report authoring, with 3-5 years in quality review.
  • Proficiency in Microsoft Office Suite (Outlook, Word, Excel).
  • Strong verbal, written, and interpersonal communication skills.
  • Organization and prioritization skills, able to multitask.
  • Ability to collaborate, build relationships, and influence across disciplines.
  • Flexible schedule and willingness to work extended hours as required.

Benefits

  • Competitive salary and variable pay.
  • Healthcare and retirement benefits.
  • Paid time off.

Work Environment

  • Full-Time, 40 hours per week (Monday to Friday), with additional hours as needed.

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