Safety Scientist II/III

🕒 5 days ago

🇷🇸 Serbia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Scientist

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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

• Plan, coordinate and deliver signal detection and product safety scientist activities • Contribute to signal detection and product safety scientist tasks across varying complexity levels • Conduct quality reviews of signal detection and product safety scientist tasks • Advise clients on safety-related issues under supervision • Lead small FSP projects • Support training and mentoring of junior colleagues • Contribute to the development of processes, tools and systems • Participate in bid defense and proposal development activities • Work within multiple company and client systems • Interact with project team members and clients • Ensure tasks comply with company policies, procedures, contractual agreements and applicable regulations • Participate in departmental initiatives and serve as a subject matter expert • Coordinate assigned project implementation, including kick-off meetings, communications, data requests, client meetings, audits, inspections, metrics and budgets • Analyze complex issues and evaluate variable factors • Determine methods and procedures for new assignments • Coordinate activities of other personnel when required • Maintain frequent contact with internal personnel and external customer representatives

🎯 Requirements

• Bachelor's degree • Previous experience comparable to 5+ years • Expertise in pharmacovigilance requirements relating to marketed products and clinical trials across all major markets • Excellent attention to detail, data interpretation and medical-scientific writing skills • Advanced critical thinking and problem-solving skills • Ability to evaluate and escalate appropriately • Solid project management skills and ability to manage multiple projects simultaneously • Ability to redress issues proactively with limited management intervention • Ability to motivate, mentor and guide less experienced staff • Robust and proactive scientific expertise • Proficient in complex project administration, including budget activities and forecasting • Excellent oral and written English language communication skills, including paraphrasing skills • Advanced computer skills and ability to work within multiple systems • Advanced Microsoft Office skills, including Outlook, Word, and Excel • Ability to maintain a positive and professional demeanor in challenging circumstances • Ability to proactively plan for likely scenarios using personal experience • Ability to work effectively within a team to attain a shared goal

🏖️ Benefits

• Continued career advancement opportunities • Award-winning training • Benefits focused on the health and wellbeing of employees • Work from home / fully remote arrangement

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