Medical Project Coordinator

🔥 7 minutes 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 visualization tools • Review data for safety trends, coding consistencies, and potential investigator-site follow-up • Identify, resolve, or escalate issues • Provide summations for safety review meetings • Review designated sections of aggregate reports • Help create and review safety and medical management plans for studies • Help manage routine project implementation, forecasting, coordination, metrics, and budget considerations • Monitor data-review status and escalate delays and risks to stakeholders and study leads • Present at business development, client, and investigator meetings • Participate in strategy and business development calls • Resolve complex problems through in-depth evaluation and offer solutions • Serve as primary point of contact for clinical/data management project teams • Assist management with training and mentoring

🎯 Requirements

• Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN • 2+ years of experience, including 2+ years of clinical safety experience in clinical research monitoring, pharmacovigilance, or a combination of both • 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 collaboratively and maintain a positive, professional demeanor • Ability to work with computer software • Ability to meet physical, environmental, attendance, multitasking, and communication requirements • Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Exposure to scientific excellence and innovation