Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Drug Safety Specialist
Job not on LinkedIn
🕒 June 22
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
📋 Description
• 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 • Assists with routine project implementation and coordination (e.g., Clinical Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee), including presentations at client/investigator meetings, and review of metrics and budget considerations • Mentors less experienced staff
🎯 Requirements
• 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 2+ years) • General understanding of pathophysiology and the disease process • Detailed knowledge of relevant therapeutic areas as required for processing AEs • 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 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.
🏖️ Benefits
• Reasonable accommodation for individuals with disabilities • Engaging work environment • Participation in the job application or interview process
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