Job Description
Step into the role of Associate II with Fortrea, focusing on patient safety solutions and adverse event report processing. Contribute to healthcare safety by managing data effectively in this office-based position.
In this role, you will process and review adverse event reports, ensuring compliance with regulations through accurate data entry and event coding via MedDRA. Collaborating with stakeholders will be a key part of your duties, alongside mentoring fellow team members and supporting audits. With your experience in pharmacovigilance, you'll be pivotal in safeguarding patient safety.
Key Responsibilities:
• Review and process clinical trial adverse event reports
• Code events using MedDRA for accurate reporting
• Submit safety reports to clients and regulatory authorities
• Maintain systems for tracking and inspections
• Provide mentorship and collaborate with clients
Requirements:
• Degree in Life Sciences preferred
• At least 2 years of safety or p...
In this role, you will process and review adverse event reports, ensuring compliance with regulations through accurate data entry and event coding via MedDRA. Collaborating with stakeholders will be a key part of your duties, alongside mentoring fellow team members and supporting audits. With your experience in pharmacovigilance, you'll be pivotal in safeguarding patient safety.
Key Responsibilities:
• Review and process clinical trial adverse event reports
• Code events using MedDRA for accurate reporting
• Submit safety reports to clients and regulatory authorities
• Maintain systems for tracking and inspections
• Provide mentorship and collaborate with clients
Requirements:
• Degree in Life Sciences preferred
• At least 2 years of safety or p...