
location_on2015, West Street, Annapolis, Anne Arundel County, Maryland, 21401, United States
At Parexel, we are dedicated to improving patient health worldwide. As a Patient Safety Associate I, you will play a vital role in supporting drug safety, clinical trials, and post-marketing surveillance activities. This position ensures full compliance with regulatory requirements and Standard Operating Procedures (SOPs) while contributing to the development of aggregate reports and study-specific safety documents.
You will be part of a global leader in Clinical Research Organization services, where you can contribute to improving patient safety while developing your career in pharmacovigilance. The role offers the flexibility to work from home in the US.
In this position, you will process Individual Case Safety Reports (ICSRs) from multiple sources with accuracy and efficiency. Your day-to-day work involves conducting comprehensive literature searches to identify safety signals, tracking regulatory information updates, and assisting in preparing regulatory submissions. You will also manage Medical and Product Dictionary activities and perform quality reviews of safety deliverables.
You will collaborate closely with team members to investigate and document late deliverable incidents, generate metrics for safety operations, and support communication between global operations and local safety affiliates. This role is crucial for maintaining adherence to international and local regulatory reporting requirements.
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Work model: Remote
2015, West Street, Annapolis, Anne Arundel County, Maryland, 21401, United States
Annapolis, Maryland
Preference for those with Veeva Safety experience.
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Skills: Drug Safety, Clinical Trials, Post-Marketing Surveillance, Regulatory Requirements, Standard Operating Procedures, Sops, Individual Case Safety Reports, Icsrs, Literature Searches, Signal Detection.
Education: Bachelor's degree in Life Sciences, Health Sciences, or Biomedical Sciences or equivalent education/experience.