Associate Safety Specialist

🔥 3 hours ago

🇮🇳 India – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Safety Specialist

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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

• Perform day-to-day Pharmacovigilance activities in a highly regulated environment • Participate in on-call duties for specific projects to ensure 24-hour case-intake coverage • Collect, monitor, assess, evaluate, research, and track safety information • Enter, code, and assess adverse-event data • Review cases and conduct follow-up activities • Track reports and perform regulatory reporting activities • Review 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 • Collaborate with project team members, client contacts, investigators, adverse-event reporters, and third-party vendors

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience comparable to 0 to 2 years • Equivalency through a combination of appropriate education, training and/or directly related experience may be considered • 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 medical terminology • Understanding of 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 • Willingness to work occasional long, varied hours • Willingness to travel occasionally domestically and/or internationally

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Scientific excellence-focused workplace