
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
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10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
• Coordinate and review safety data, utilizing line listings, company dashboards and/or other visualization tools • Review data for safety trends, coding consistencies, and potential follow up with investigator sites • Identify potential issues and resolve or escalate as appropriate • Review safety data and may provide summations for safety review meetings • May review designated sections of aggregate reports • May help to create/review safety and medical management plan(s) on studies and ensures that the processes included in plan documents are reflective of the contract and services requested • May help manage routine project implementation, forecasting and coordination, including review of metrics and budget considerations • Monitor the status of the data review and escalate any delays and/or risks to all stakeholders, including study leads • May present at business development, client, and investigator meetings and participate in strategy/business development calls • Resolve complex problems through in-depth evaluation of various factors and offers solutions • May serve as the primary point of contact for clinical/data management project teams • May assist management in training and mentoring
• Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN • Previous experience providing the knowledge, skills, and abilities to perform the job (comparable to 2+ years) • 2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)
• Health insurance • Professional development opportunities
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