Medical Project Coordinator

🔥 3 hours ago

🇵🇭 Philippines – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

Where this job comes from

Posted on Thermo Fisher Scientific's careers page, not through a job board

First seen by Remote Rocketship 3 hours ago

Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 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 potential issues • Provide safety-data summaries for safety review meetings • Review designated sections of aggregate reports • Help create and review safety and medical management plans for studies • 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 • Participate in strategy and business development calls • Resolve complex problems through in-depth evaluation and offer solutions • Serve as a 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 previous experience comparable to the role • 2+ years of clinical safety experience, including clinical research monitoring, pharmacovigilance, or a combination of both • Equivalency combining appropriate education, training, and/or directly related experience may be considered • 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 • Ability to maintain a positive and professional demeanor in challenging circumstances • Ability to work upright and/or stationary for 6–8 hours per day • Ability to perform repetitive hand movements and frequent mobility • Ability to lift and carry objects weighing up to 15–20 lbs • Ability to use computer software • Regular and consistent attendance

🏖️ Benefits

• Collaboration and development opportunities • Opportunity to contribute to scientific excellence and patient safety • Global team environment

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