Medical Project Coordinator

🔥 3 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 consistency, and potential investigator-site follow-up • Identify, resolve, or escalate safety-data issues • Provide summations for safety review meetings • Review designated sections of aggregate reports • Help create and review safety and medical management plans • Help manage 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 and provide solutions • Serve as primary 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 (clinical research monitoring, pharmacovigilance, or a combination) • 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 in an office/laboratory and/or clinical environment • Ability to use a variety of computer software • Ability to meet physical, mobility, lifting, attendance, and multitasking requirements • Exposure to biological fluids, infectious organisms, electrical office equipment, and use of required personal protective equipment

🏖️ Benefits

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