Patient Safety Specialist I

Remote Jobs; Brasil; Teletrabalho; USD 61.000 - 73.000; Tempo integral

Resumo da oferta

A leading clinical research organization seeks a Patient Specialist I for a remote role focused on safety data collection for clinical trials. Responsibilities include follow-up outreach to healthcare professionals, processing adverse event reports, and maintaining data quality and compliance. The ideal candidate will have a degree in Life Sciences and 4+ years' experience in pharmacovigilance, with proficiency in Argus safety database and MedDRA coding.

Serviços

Comprehensive medical benefits

401(K) plan

Paid time off (PTO)

Qualificações

• Minimum 4 years of pharmacovigilance or safety experience.
• Experience in US case processing.
• Proficient in coding adverse events.

Responsabilidades

• Conduct follow-up calls to collect safety data.
• Process adverse event reports from clinical trials.
• Enter data into safety databases and code events.

Conhecimentos

Attention to detail

Strong communication skills

Experience with telephonic query follow up

Formação académica

Degree in Life Sciences, Nursing, or Pharmacy

Ferramentas

Argus safety database

MedDRA coding

Descrição da oferta de emprego

As one of the largest Clinical Research Organizations in the world.

Great opportunity for US based PV Specialist. We're looking for a detail-oriented Patient Specialist I to support safety data collection and follow-up for clinical trials and post-marketing activities. This remote role involves outbound outreach to healthcare professionals and consumers to gather and process adverse event information in compliance with regulatory standards.

This is a full-time, remote based position in the US.

WHAT YOU WILL DO

• Conduct follow-up calls and outreach to collect safety data.
• Process and review adverse event reports from clinical trials and spontaneous sources.
• Identify and query missing safety information.
• Enter data into safety databases and code events using MedDRA.
• Write patient narratives and ensure data quality and compliance.

YOU NEED TO BRING...

• Degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum 4 years of pharmacovigilance or safety including US case processing experience.
• Strong communication skills and attention to detail.
• Experience with telephonic query follow up, ICSR processing including MedDRA coding
• Proficient with Argus safety database

Pay Range: $72,200

Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.

Application Deadline: August 4, 2025

This position is not eligible for sponsorship.

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