Lead Medical Project Coordinator

🕒 July 15

🇵🇭 Philippines – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 20%

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

• Lead the management, coordination and evaluation of medical projects • Work independently to perform and/or lead first pass review of safety data • Proactively identify and resolve/escalate potential issues • Initiate and lead initiatives to improve processes regarding medical monitoring • Manage project implementation, coordination, maintenance and close out • Serve as the primary point of contact for clinical project teams • Create and maintain safety and medical management plan(s) • Monitor project financial status and escalates any financial or operational risks • Train and develop new team members • Resolve complex problems through in-depth evaluation of various factors

🎯 Requirements

• Bachelor's degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN • 8+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of both) • Superior knowledge of GCPs for medical oversight of clinical trials • Advanced knowledge of drug development and safety reporting • Extensive knowledge of safety data trending to include coding • Good knowledge of biostatistics, data management and clinical procedures • Exceptional problem solving and critical thinking skills • Exceptional project management and budget skills • Excellent mentoring skills and ability to train and lead others • Exceptional oral and written communication skills

🏖️ Benefits

• Health and wellbeing support • Resources for individual career goals • Opportunities for collaboration and development