
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.
🕒 August 26
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship August 26
Still open on Thermo Fisher Scientific's site. Checked 6 hours ago.

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.
• Perform day-to-day pharmacovigilance activities in a highly regulated environment with strict timelines • Participate in on-call duties for specific projects to ensure 24-hour case-intake coverage from investigative sites • Collect, monitor, assess, evaluate, research, and track safety information • Perform data entry, coding, adverse-event assessment, case review, follow-up, report tracking, and regulatory reporting • Review regulatory/pharmacovigilance publications and information sources to stay current on regulations, practices, procedures, and proposals • Maintain medical understanding of applicable therapeutic areas and disease states • Review cases for quality, consistency, and accuracy, including peer reports • Prepare and maintain regulatory safety reports • Assist with routine project implementation and coordination, including clinical trials and Endpoint Assessment Committee/Data Safety Monitoring Committee activities • Present at client and investigator meetings • Review metrics and budget considerations • Mentor less experienced staff • Assist with departmental and project-specific procedures and processes • Prepare for and attend audits, kick-off meetings, and investigator meetings • Collaborate with project team members, client contacts, investigators, adverse-event reporters, and third-party vendors
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 2+ years of previous experience providing the knowledge, skills, and abilities to perform the job • Combination of appropriate education, training and/or directly related experience may be considered sufficient to meet the role requirements • General understanding of pathophysiology and the disease process • Detailed knowledge of relevant therapeutic areas as required for processing adverse events • 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 literacy and ability to work within multiple databases • Previous exposure to Microsoft Office packages, including Outlook, Word, and Excel • Understanding of compliance with procedural documents and regulations • Ability to manage and prioritize varied 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 • Willingness and ability to work night shift, based on the posting title and schedule context
• Global team environment • Collaboration and development opportunities • Occasional domestic and/or international travel opportunities
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