Clinical Research Associate I

🔥 2 hours ago

🇲🇽 Mexico – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 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

• Deliver clinical studies at allocated sites and participate in local study teams • Act as the main contact with study sites and monitor study conduct • Prepare, initiate, monitor and close assigned clinical study sites • Contribute to investigator selection • Support study start-up and regulatory maintenance, including site qualification visits and submissions to EC/IRB and regulatory authorities • Train, support and advise investigators and site staff on study-related matters and RBQM principles • Confirm required site staff training and inspection readiness • Participate in local study team and national investigator meetings • Drive site performance and resolve or escalate study-related issues • Update CTMS and other systems with site data • Manage study supplies, drug supplies and drug accountability • Perform remote and on-site monitoring visits, remote data checks, SDR, CRF review and SDV • Perform site quality risk assessments and adapt monitoring intensity • Ensure timely data query resolution and work with data management on data quality • Ensure accurate and timely reporting of Serious Adverse Events and follow-ups • Prepare and finalize monitoring visit reports and provide feedback to Principal Investigators • Follow up on outstanding site actions • Escalate systematic or serious quality, privacy and compliance issues • Assist sites in maintaining inspection-ready ISFs • Support audits and regulatory inspections • Collect and upload essential documents to the eTMF and support QC checks • Ensure study documents are ready for final archiving • Provide research-related market feedback • Ensure compliance with AstraZeneca ethics, policies, procedures and applicable legislation • Collaborate with local MSLs as directed

🎯 Requirements

• 0–2 years of prior relevant experience • Good knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Written and verbal communication skills • Good command of English • Degree in a scientific discipline or healthcare • Equivalent combination of education, training and experience may be accepted in lieu of a degree

🏖️ Benefits

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

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