Medical Project Coordinator

🔥 17 hours ago

🇷🇸 Serbia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

👻 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

• Coordinate and review safety data using line listings, company dashboards, and/or visualization tools • Review data for safety trends, coding consistencies, and potential investigator-site follow-up • Identify potential issues and resolve or escalate them as appropriate • Review safety data and provide summations for safety review meetings • Review designated sections of aggregate reports • Help create and review safety and medical management plans for studies, as applicable • Ensure plan processes reflect contracted services • Help manage routine project implementation, forecasting, and coordination • Review metrics and budget considerations • Monitor data-review status and escalate delays or risks to stakeholders and study leads • Present at business development, client, and investigator meetings as needed • Participate in strategy and business development calls • Resolve complex problems through in-depth evaluation and offer solutions • Serve as the primary point of contact for clinical/data management project teams as needed • Assist management with training and mentoring

🎯 Requirements

• Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN • Previous experience comparable to 2+ years • 2+ years of clinical safety experience, including clinical research monitoring, pharmacovigilance, or a combination of both • Equivalency may be considered through a combination of appropriate education, training, and/or directly related experience • Knowledge of GCPs for medical oversight of clinical trials and SAE processing • Knowledge of drug development and safety reporting • Knowledge of safety data trending, including coding • Working knowledge of biostatistics, data management, and clinical procedures • Strong problem-solving and critical-thinking skills • Good oral and written communication skills • Good attention to detail • Ability to work in a collaborative team environment • Ability to maintain a positive and professional demeanor in challenging circumstances

🏖️ Benefits

• Collaboration and development opportunities • Opportunity to contribute to scientific excellence and breakthrough healthcare solutions