CRA / Sr. CRA

🔥 2 minutes ago

🇵🇪 Peru – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 15%

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

• Perform and coordinate clinical monitoring and site management activities • Conduct remote and on-site visits to assess protocol and regulatory compliance • Manage required clinical trial documentation and ensure audit readiness • Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs • Monitor investigator sites using a risk-based monitoring approach • Identify site process failures, perform root cause analysis, and implement corrective/preventive actions • Ensure data accuracy through SDR, SDV, and CRF review • Assess investigational product inventory and records • Document observations and escalate deficiencies and issues through resolution • Maintain regular contact with investigative sites between monitoring visits • Participate in investigator payment processes and investigator meetings • Identify potential investigators and initiate clinical trial sites • Perform trial closeout and retrieve trial materials • Ensure essential documents are complete and properly maintained • Conduct on-site file reviews • Track trial status and provide progress updates to the Clinical Team Manager • Update study systems, including Clinical Trial Management Systems • Facilitate communication between investigative sites, the client company, and the PPD project team • Respond to company, client, and regulatory requirements, audits, and inspections • Complete expense reports and timesheets • Assist with project publications and tools • Contribute to project initiatives and process improvement

🎯 Requirements

• Bachelor's degree in a life sciences related field • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 1+ years as a clinical research monitor • International monitoring experience • Frequent travel, generally 60–80%, with possible extended overnight stays • No restriction to travel internationally • Lives within an international airport location • Ability to conduct remote or on-site clinical monitoring visits • Knowledge of ICH-GCP guidelines, applicable regulations, and SOPs • Experience with risk-based monitoring, root cause analysis, critical thinking, and problem-solving • Experience with source document review (SDR), source data verification (SDV), and CRF review • Ability to assess investigational product inventory and records • Clinical trial site management and essential document management experience • Familiarity with clinical trial management systems • Ability to respond to regulatory requirements, audits, and inspections

🏖️ Benefits

• Fully remote work mode • Standard Monday–Friday work schedule

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