Drug Safety Associate

myBridge Corporation; Iowa (LA); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Dental Insurance

Vision Insurance

401K

Medical Insurance

Job summary

myBridge Corporation is seeking a Drug Safety Associate to support pharmacovigilance activities and ensure the safety of pharmaceutical products throughout their lifecycle.

The role involves reviewing adverse event reports, monitoring product safety data, and maintaining pharmacovigilance databases to ensure FDA, EMA, and global regulatory compliance. Collaboration with clinical research teams is essential to evaluate safety information and manage risk.

Qualifications

• Bachelor's degree in Pharmacy, Life Sciences, Nursing, Medicine, or related field.
• 1–3 years of pharmacovigilance or clinical safety experience.
• Experience with safety reporting and regulatory compliance.

Responsibilities

• Process adverse event reports.
• Evaluate drug safety information.
• Prepare safety reports.
• Monitor global safety trends.
• Ensure regulatory compliance.
• Collaborate with clinical teams.
• Review medical documentation.

Skills

Drug Safety

FDA Regulations

GCP

MedDRA

Medical Terminology

Clinical Research

Data Entry

Attention to Detail

Communication

Education

Bachelor's degree in Pharmacy, Life Sciences, Nursing, Medicine, or related field

Job description

Dental Insurance, Vision Insurance, 401K, Medical Insurance

Full-Time | On-site

Job Description

We are seeking a dedicated Drug Safety Associate to support pharmacovigilance activities and ensure the safety of pharmaceutical products throughout their lifecycle. The successful candidate will review adverse event reports, monitor product safety data, maintain pharmacovigilance databases, and ensure compliance with FDA, EMA, and global regulatory requirements.

The Drug Safety Associate will collaborate with clinical research teams, regulatory affairs professionals, medical reviewers, and quality assurance personnel to evaluate safety information and contribute to risk management activities.

Responsibilities

• Process adverse event reports.
• Evaluate drug safety information.
• Ensure regulatory compliance.
• Prepare safety reports.
• Collaborate with clinical teams.
• Review medical documentation.
• Monitor global safety trends.

Education

• Bachelor's degree in Pharmacy, Life Sciences, Nursing, Medicine, or related field.

Required Skills

• Drug Safety
• FDA Regulations
• GCP
• MedDRA
• Medical Terminology
• Clinical Research
• Data Entry
• Attention to Detail
• Communication

Experience

• 1–3 years of pharmacovigilance or clinical safety experience.