Medical Project Coordinator

🕒 July 15

🇵🇭 Philippines – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ 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

• Coordinate and review safety data, utilizing line listings and/or other visualization tools. • Identify potential issues and resolve or escalate as appropriate. • Review safety data and provide summations for safety review meetings. • Help manage routine project implementation, forecasting and coordination. • Monitor the status of the data review and escalate any delays and/or risks to stakeholders. • Resolve complex problems through in-depth evaluation of various factors and offers solutions.

🎯 Requirements

• Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN • Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years) • 2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance) • Knowledge of GCPs for medical oversight of clinical trials and SAE processing • Knowledge of drug development and safety reporting • Knowledge of safety data trending to include coding • Working knowledge of biostatistics, data management and clinical procedures

🏖️ Benefits

• Personal protective equipment required such as protective eyewear, garments and gloves. • Regular and consistent attendance. • Global team that values passion, innovation, and a commitment to scientific excellence. • Collaborate and develop in an environment where contributions make a difference.