Clinical Research Associate I

🔥 15 minutes ago

🇨🇱 Chile – 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.

Apply Now

Find Similar Remote Jobs

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 assigned clinical studies at allocated sites as an active participant in local study teams • Serve as the main contact for study sites and monitor study conduct • Prepare, initiate, monitor, and close assigned study sites • Contribute to investigator selection and, where applicable, study start-up and regulatory maintenance • Train, support, and advise investigators and site staff on study-related matters and RBQM principles • Confirm required site-staff training and maintain inspection readiness • Participate in local study team and national investigator meetings • Drive site performance, identify and resolve study issues, and escalate them appropriately • Update CTMS and other systems with site data • Manage study supplies, drug supplies, and drug accountability • Perform monitoring visits, remote data checks, SDR, CRF review, and SDV according to the Monitoring Plan • Perform site quality risk assessments and adapt monitoring intensity • Ensure timely data query resolution and accurate Serious Adverse Event reporting • Prepare and finalize monitoring visit reports and provide feedback to Principal Investigators • Follow up on outstanding site actions • Escalate quality issues, data privacy breaches, and compliance issues • Assist sites in maintaining inspection-ready Investigator Site Files • Support audits and regulatory inspections • Collect and upload essential documents to the eTMF and prepare study documents for archiving • Provide research-related market feedback on sites, investigators, and competing studies • Ensure compliance with AstraZeneca policies, ethical standards, 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 health care, or equivalent combination of education, training and experience accepted in lieu of degree • Ability to conduct monitoring visits, including remote and on-site visits • Knowledge of study start-up, regulatory maintenance, site management, clinical data review, and quality risk assessment processes

🏖️ Benefits

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

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume