Clinical Research Associate I, Bilingual French

🔥 2 minutes ago

🇨🇦 Canada – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Conduct and coordinate clinical monitoring and site management activities • Perform remote and on-site visits to assess protocol and regulatory compliance • Manage sponsor procedures and guidelines across different monitoring environments • Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations and SOPs • Maintain audit readiness and collaborative relationships with investigational sites • Monitor investigator sites using risk-based monitoring, root cause analysis and corrective/preventive actions • Ensure data accuracy through source document review, source data verification and case report form review • Assess investigational products through inventory and records review • Document observations in reports and letters and escalate deficiencies through resolution • Maintain contact with sites between monitoring visits to confirm protocol adherence and issue resolution • Participate in investigator payments, investigator meetings, site identification, site initiation, trial closeout and trial-material retrieval • Ensure essential documents are complete and conduct on-site file reviews • Track trial status and provide progress reports; maintain clinical trial management systems • Facilitate communication among sites, the client company and internal project teams • Respond to company, client and regulatory requirements, audits and inspections • Complete expense reports and timesheets • Support project publications, tools, process-improvement initiatives and other project work

🎯 Requirements

• Bachelor's degree in a life sciences related field, or Registered Nursing certification, or equivalent relevant formal academic/vocational qualification • Minimal clinical monitoring experience comparable to 2 years (24 months) in clinical trials, medical terminology, medical research, clinical research, health care, or a health sciences field with formal training in medical terminology and anatomy • Valid driver's license where applicable • Equivalency may consist of a combination of appropriate education, training and/or directly related experience • Basic medical/therapeutic area knowledge and understanding of medical terminology • Working knowledge of ICH GCPs, applicable regulations and procedural documents, or ability to attain and maintain it • Good oral and written communication skills with medical personnel • Good interpersonal, organizational and time management skills • Critical thinking, root cause analysis and problem-solving skills • Ability to manage Risk Based Monitoring concepts and processes • Ability to work independently or as part of a team • Solid knowledge of Microsoft Office and ability to learn appropriate software • Good English and French language and grammar skills • Ability to travel frequently, generally 60–80%, including possible extended overnight stays • Ability to work in office, laboratory, clinical and/or home office environments and use required personal protective equipment

🏖️ Benefits

• Fully remote work arrangement • Full-time employment • Standard Monday–Friday work schedule • Frequent travel expenses likely covered through employer processes • Personal protective equipment provided/required, including protective eyewear, garments and gloves