Senior CRA – Level I

🔥 24 minutes ago

🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

🧪 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 assigned clinical studies at allocated sites and participate in local study teams • Collaborate with CRAs and the Local Study Team/Local Study Associate Director to achieve study commitments • Act as the main contact for study sites and monitor study conduct • Prepare, initiate, monitor, and close assigned clinical study sites • Contribute to investigator selection and national investigator meetings • Support study start-up and regulatory maintenance, including site qualification visits, document preparation, and submissions to EC/IRB and regulatory authorities • Train, support, and advise investigators and site staff on study-related matters and Risk Based Quality Management principles • Ensure sites are inspection ready and required training is completed and documented • Drive site performance, resolve study issues, and escalate issues appropriately • Update CTMS and other systems with site data • Manage study, drug, and drug-accountability supplies • Perform remote and onsite monitoring visits and remote data checks • Perform Source Data Review, Case Report Form review, and Source Data Verification • Conduct site quality risk assessments and adapt monitoring intensity • Ensure timely data query resolution and collaborate with data management on study data quality • Ensure accurate and timely Serious Adverse Event reporting and follow-up • Prepare and finalize monitoring visit reports and provide feedback to Principal Investigators • Follow up on outstanding site actions • Escalate systematic or serious quality issues, data privacy breaches, CSP, or ICH-GCP 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 support quality-control checks • Ensure study documents are ready for final archiving and local eTMF completion • Provide research-related intelligence on sites, investigators, and competing studies • Collaborate with local MSLs as directed

🎯 Requirements

• Minimum 3–5 years' experience as a monitor • Ability to work independently and monitor all stages of a study across different phases • Special therapeutic expertise in oncology • Ability to take on LST tasks and support LST coordination or document preparation as required • Ability to travel internationally as required • Valid driving license • Completion and documentation of required training, including ICH-GCP training, prior to and throughout the study • Knowledge of ICH-GCP, AZ Procedural Documents, international guidelines, and relevant local regulations • Compliance with AstraZeneca’s Code of Ethics, company policies, procedures, and applicable legislation

🏖️ Benefits

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

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