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A leading Clinical Research Organization is seeking a detail-oriented Patient Specialist I for a remote role. This position involves conducting follow-up calls for safety data collection, processing adverse event reports, and ensuring compliance with regulatory standards. Candidates should have a degree in Life Sciences and a minimum of 4 years of relevant experience. Comprehensive benefits and a competitive salary of $72,200 are offered.
As one of the largest Clinical Research Organizations in the world.
We're looking for a detail-orientedPatient 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.
Support quality control, training, and client communications
Will travel up to 5% travel as needed.
YOU NEED TO BRING...
Degree in Life Sciences, Nursing, Pharmacy, or related field.
Minimum4 years of pharmacovigilance or safety experience.
Strong communication skills and attention to detail.
Experience with telephonic outreach, MedDRA coding, and safety databases.
Pay Range:$72,200
Benefits:All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor 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:July 11, 2025
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