A global research company is looking for a Senior Pharmacovigilance Associate. The successful applicant will be responsible for producing a safety management plan for designated studies. This is a fully remote position.
Participate in meetings with clients and internal stakeholders
Verify the accuracy and completeness of the incoming
Conduct quality control on SAEs that other PV Associates have processed
Handle data input into the safety database
Monitor incoming safety information
Create inquiries to find any missing or unclear data
Bachelor’s degree or equivalent in nursing or science-related industry
More than 3 years of experience in pharmacovigilance
Skilled in MS Office Suite
Proficient in written and verbal English
About the Company:
An international research organisation with the goal of finding innovations in medical science. The company oversees clinical trials across various countries.
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