Pharmacovigilance Assistant I

Jobtailor; São Paulo; Presencial; BRL 33 000 - 56 000; Tempo integral

Resumo da oferta

Jobtailor is seeking a Pharmacovigilance Support Associate in São Paulo to assist in collecting, reviewing, and processing adverse event reports for clinical trials and marketed products. You will ensure timely data entry into pharmacovigilance databases, help prepare safety reports for regulators and sponsors, and maintain thorough documentation in a fast-paced, regulated environment.

This role requires attention to detail, strong organizational and communication skills, and a lawful right to

Qualificações

• Basic understanding of pharmacovigilance principles and regulatory requirements is preferred
• Strong attention to detail and organizational skills
• Effective communication and collaboration skills with accurate documentation
• Ability to work in a fast-paced, regulated environment ensuring safety guidelines compliance

Responsabilidades

• Support collection, review, and processing of adverse event reports
• Ensure timely and accurate data entry into pharmacovigilance databases
• Assist in preparing and submitting safety reports to regulatory authorities and sponsors
• Collaborate with cross-functional teams to maintain safety compliance
• Maintain detailed records and documentation related to pharmacovigilance activities

Conhecimentos

Pharmacovigilance principles

Attention to detail

Organizational skills

Effective communication

Regulatory compliance

Ferramentas

Pharmacovigilance Databases

Descrição da oferta de emprego

• Support the collection, review, and processing of adverse event reports related to clinical trials and marketed products
• Ensure timely and accurate data entry of safety information into pharmacovigilance databases
• Assist in preparing and submitting safety reports to regulatory authorities and sponsors, as required
• Collaborate with cross-functional teams to maintain compliance with safety regulations and company protocols
• Maintain detailed records and documentation related to pharmacovigilance activities and safety reporting

Requirements

• Basic understanding of pharmacovigilance principles and regulatory requirements is preferred
• Strong attention to detail and organizational skills, with the ability to manage multiple tasks efficiently
• Effective communication and collaboration skills, with a focus on maintaining accuracy in documentation and reporting
• Ability to work in a fast-paced, regulated environment, ensuring compliance with safety guidelines and protocols
• Legal right to work in the country where the role is based

Core Competencies

Demonstrates a solid understanding of pharmacovigilance principles and regulatory requirements, with strong attention to detail and organizational skills to manage multiple tasks efficiently in a fast-paced, regulated environment.

Highest-signal resume keywords

• Pharmacovigilance Principles
• Regulatory Requirements
• Data Entry Accuracy
• Safety Reporting
• Collaboration Skills

Soft Skills

• Attention To Detail
• Organizational Skills
• Effective Communication
• Collaboration

Industry Keywords

• Adverse Event Reports
• Safety Information
• Compliance
• Safety Guidelines
• Documentation

Tools & Technologies

• Pharmacovigilance Databases