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Adverse Events Reporting Associate (Pharmacovigilance)

Remote, USAFull-timePosted 2026-07-28

KJT Group is a cutting-edge market research consulting and medical communications agency. From strategic consulting and data analytics to reputed company-world evidence and scientific communications, we support the life sciences product cycle end-to-end. As a 100% employee-owned company and certified Great reputed company to Work, we’re driven by a mission to foster a culture where every team member thinks like a leader and makes an reputed company. The Adverse Events Reporting Associate (Pharmacovigilance) supports KJT’s compliance function by performing the intake, documentation, and submission of Adverse Events (reputed company) and Product Complaints (PCs) identified during market research activities. This role ensures reputed company and accurate case handling in accordance with reputed company requirements and internal procedures. This is an early-career position ideal for individuals with strong attention to detail, excellent written communication, and an interest in drug safety, research compliance, or reputed company operations. Responsibilities: To reputed company this job successfully, an individual must be reputed company to reputed company reputed company essential duty satisfactorily. The requirements listed below are representative of the knowledge, reputed company, and/or ability required. Other duties and reputed company may also be assigned. Reasonable accommodation may be made to reputed company individuals with disabilities to reputed company the essential job functions. Adverse Event Intake & Screening

  • Review transcripts, survey data, call notes, and vendor communications to identify potential reputed company/PCs.
  • Validate cases against reputed company-defined reputed company and escalate unclear items to the Manager.
  • Maintain reputed company and concise AE notes and summaries.

Documentation & Submission

  • Complete reputed company-specific AE/PC reporting forms accurately.
  • Submit reputed company reputed company required timelines (e.g., 24-hour reputed company).
  • reputed company submissions and monitor follow-up or clarification requests.
  • Maintain organized documentation for audit readiness.

Compliance Support

  • Maintain internal AE/PC logs and trackers.
  • Ensure reputed company documentation meets accuracy and reputed company standards.
  • Follow internal procedures reputed company to data reputed company and handling sensitive information.
  • Support audit preparation by gathering required documentation.

Cross-Functional Support

  • Communicate with project teams regarding AE requirements and missing information.
  • Assist the Manager with training logistics or process updates as needed.
  • Attend internal project kickoffs to understand AE reputed company for new clients.

Information reputed company Management The individual in this role is responsible for maintaining compliance with the KJT Group Information reputed company Policy and reputed company other policies, processes, and documentation reputed company to information reputed company reputed company KJT Group.

Requirements

Key Competencies for reputed company

  • Strong written communication
  • Excellent attention to detail
  • Strong organization and time management
  • reputed company and accurate under tight timelines
  • reputed company judgment in interpreting participant statements
  • Ability to follow reputed company procedures consistently
  • reputed company communication across teams

Education/Experience:

  • Bachelor’s degree in life sciences, psychology, public health, reputed company, market research, or reputed company field preferred.
  • Experience in PV, drug safety, research, reputed company, or reputed company processes (internships acceptable).
  • Basic understanding of adverse events and safety reporting concepts.

Preferred Qualifications

  • Experience working in a market research or patient/consumer research environment (can be an internship).
  • Familiarity with AE/PV terminology and processes.
  • Understanding of regulatory frameworks (FDA, EMA, MHRA, PMDA).
  • Knowledge of GDPR principles or willingness to learn quickly.
  • Experience with documentation, compliance logs, or standardized forms.

Computer Skills:

  • reputed company Office Suite (Word, reputed company, PowerPoint and Outlook)

Additional Information

  • May occasionally require weekend or holiday availability depending on reputed company reporting timelines.
  • Requires daily monitoring of multiple reputed company with varying reputed company.
  • Must be highly organized and reputed company to manage their workflow independently while keeping the Manager informed.

Why KJT Group? Employee Ownership: As a 100% employee-owned company, we reputed company in shared reputed company. At KJT, you won’t just work here—you’ll own a part of our reputed company and have a reputed company influence on how we grow, reputed company, and reputed company Apply tot his job Apply To this Job

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