Thermo Fisher Scientific
Location
São Paulo (estado) | Brazil
Job description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeEssential Functions
Performs day-to-day PV activities. May participate in on-call duties for specific
projects to ensure 24-hr coverage for intake of cases from investigative sites.
Reviews regulatory/pharmacovigilance publications and information sources to
keep updated on current regulations, practices, procedures and proposals.
Maintains medical understanding of applicable therapeutic area and disease
states.
Reviews cases entered for quality, consistency and accuracy, including review of
peer reports.
Prepares and maintains regulatory safety reports.
Qualifications:
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Knowledge, Skills and Abilities:
Strong critical thinking and problem solving skills
Good oral and written communication skills including paraphrasing skills
Good command of English and ability to translate information into local language where required
Computer literate with the ability to work within multiple databases
Previous exposure to Microsoft Office packages (including Outlook, Word, and Excel)
Understanding of medical terminology
Understanding the importance of and compliance with procedural documents and regulations
Ability to manage and prioritize a variety of tasks and meet strict deadlines with limited supervision
Strong attention to detail
Ability to maintain a positive and professional demeanor in challenging circumstances
Ability to work effectively within a team to attain a shared goal
Job tags
Salary