Worldwide Clinical Trials is seeking an Associate II in Pharmacovigilance to join their remote team in Brazil. The ideal candidate will have at least three years of pharmacovigilance experience and a strong understanding of clinical assessment and international regulations
Job Summary
The role involves serving as a Lead PV Associate on moderate to large sized studies that are moderate to complex in scope of work.
Candidates must author Safety Management Plans for assigned studies and attend Investigator Meetings.
Worldwide Clinical Trials is a global team committed to improving lives through pioneering approaches to curing persistent diseases.
Matching Summary
Match Score: 85
Worldwide Clinical Trials is seeking an Associate II in Pharmacovigilance to join their remote team in Brazil. The ideal candidate will have at least three years of pharmacovigilance experience and a strong understanding of clinical assessment and international regulations.
Skills & Requirements
Must-have
Strong understanding of medical terminology
Experience with international regulations
Proficiency in safety database management
Ability to handle multiple competing priorities
Nice-to-have
Excellent written and verbal communication skills
Commitment to diversity and inclusion
Willingness for potential limited travel
Key Requirements
Minimum of 3 years of pharmacovigilance experience
Bachelor's degree in science related field or nursing