Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for a remote position in Mexico or Brazil. The role involves managing the collection, evaluation, and reporting of serious adverse event data, requiring extensive experience in pharmacovigilance
Job Summary
Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements.
Author Safety Management Plan for assigned studies and perform QC of SAEs processed by other PV Associates.
We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
Matching Summary
Match Score: 85
Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for a remote position in Mexico or Brazil. The role involves managing the collection, evaluation, and reporting of serious adverse event data, requiring extensive experience in pharmacovigilance.
Skills & Requirements
Must-have
SAE data collection and processing
Safety Management Plan authoring
Regulatory reporting and submissions
Medical and scientific terminology
International regulations and reporting
Nice-to-have
Positive attitude and diplomacy
Global customer interaction
Adaptability and flexibility
Key Requirements
Bachelor's degree in science-related field or equivalent
Minimum of 5 years of pharmacovigilance experience