Hybrid Pharmacovigilance Associate — Safety Data & SAEs

Piper Companies; Bethesda (MD); Hybrid; USD 34,000 - 40,000; Full time

Benefits offered by this job

Medical/Dental/Vision insurance

401K

Sick leave

Job summary

Piper Companies is seeking an S & P Associate to join a clinical research organization in Bethesda, MD. The role focuses on safety data management, SAE processing, and documentation control within a hybrid work model.

The position requires a life sciences background with relevant internship experience and at least 1 year in clinical research or safety. It offers a competitive hourly rate and comprehensive benefits in a regulated, collaborative environment.

Qualifications

• Bachelor's degree with 1+ years of clinical research or safety experience
• 1+ years of experience in a clinical research environment or bioethics setting
• Knowledge of medical terminology and drug/vaccine development process or clinical trials

Responsibilities

• Manage and process Serious Adverse Events (SAEs) per project requirements.
• Maintain safety documentation, electronic files, and tracking systems.
• Track and process DMC queries and generate safety data reports.
• Process safety narratives, assist with MedDRA coding, QC AE submissions, and distribute safety information.

Skills

Clinical research

Safety data analysis

Regulatory compliance

Education

Bachelor's degree in life sciences

Master's degree in life sciences (with internship)

Tools

SAS

SPSS

Microsoft Excel

Microsoft Word

SharePoint

Job description

Piper Companies is seeking an S & P Associate to join a clinical research organization in Bethesda, MD. The role focuses on safety data management, SAE processing, and documentation control within a hybrid work model.

The position requires a life sciences background with relevant internship experience and at least 1 year in clinical research or safety. It offers a competitive hourly rate and comprehensive benefits in a regulated, collaborative environment.