Drug Specialist I, Patient Safety Solutions

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

We're looking for a detail-oriented Drug 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.

• Minimum 4 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 31, 2025

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Learn more about our EEO & Accommodations request here.