FSP Pharmacovigilance Coordinator – Night Shift

🔥 2 hours ago

🇵🇭 Philippines – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.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

🧬 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 timely review of protocol inquiries, serious and non-serious adverse events, diagnostics and Data Safety Monitoring Board data • Track required data and generate reports for clients, project teams and external vendors • Represent the DSMB/EAC Coordination Team at global and domestic committee meetings • Coordinate meeting logistics and assist with facilitation • Liaise with internal and external parties to implement projects • Prepare and review Confidentiality Disclosure Agreements, Letters of Intent and Member Agreements • Coordinate internal and external contractual approvals • Compile adjudication dossiers and submit follow-up to investigative sites • Coordinate and facilitate project meetings, draft minutes, and distribute meeting materials • Manage project training and program-file setup, maintenance and archiving • Ensure pharmacovigilance programs remain audit ready • Identify and redact subject identifiers, retrain sites and escalate recurring issues to Data Privacy • Perform data entry in databases, tracking systems and budget management systems • Perform system reconciliations and identify issues that may affect project timelines • Oversee expenses and manage translations within budget parameters • Answer incoming hotline calls and coordinate department functions • Support activities performed by the local office • Provide training to junior staff

🎯 Requirements

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Technical positions may require a certificate • At least 2 years of comparable previous experience • Equivalent combination of appropriate education, training and/or directly related experience may be considered • Strong problem-solving skills • Ability to work independently with minimal supervision • Ability to build strong relationships • Ability to analyze project-specific data/systems for accuracy and efficiency • Effective liaison and respectful, diplomatic communication with clients, management, project team members and internal staff • Effective oral, written communication and interpersonal skills • Excellent computer skills, including MS Office (Word, Excel, PowerPoint, Access) • Ability to prioritize and perform multiple tasks under strict deadlines • Strong attention to detail and accuracy • Flexibility to reprioritize workload according to changing project timelines • Working knowledge of applicable FDA Regulations, ICH Good Clinical Practices, and organizational/client SOPs and WPDs for non-clinical/clinical project implementation, execution and closeout

🏖️ Benefits

• Fully remote work mode • Standard Monday–Friday schedule • Potential travel to site locations on rare occasions • Training opportunities, including training to junior staff

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