Assoc Safety Spec-
4 weeks ago
Key Responsibilities:
- Perform day-to-day PV activities
- Participate in on-call duties for specific projects
- Review regulatory/pharmacovigilance publications and information sources
- Maintain medical understanding of applicable therapeutic area and disease states
- Review cases entered for quality, consistency and accuracy
- Prepare and maintain regulatory safety reports
Qualifications:
- 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)
Requirements:
- 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
Equal Employment Opportunity:
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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