Parexel एक वैश्विक क्लिनिकल रिसर्च संगठन है, जो नई दवाओं के विकास के दौरान बायोफार्मास्यूटिकल कंपनियों को सेवाएँ प्रदान करता है। इसका कार्य चरण I–IV क्लिनिकल परीक्षणों, पोर्टफोलियो और परीक्षण प्रबंधन, नियामक रणनीति, बाज़ार तक पहुँच तथा जीवनचक्र योजना तक फैला हुआ है। 21,000 से अधिक पेशेवरों के साथ, Parexel क्लिनिकल, नियामक और उपचार-विज्ञान संबंधी विशेषज्ञता को मरीजों की अंतर्दृष्टि और नवीन परीक्षण डिज़ाइनों के साथ जोड़ता है। कंपनी ऑन्कोलॉजी, न्यूरोसाइंस और दुर्लभ रोगों सहित विभिन्न क्षेत्रों में अनुसंधान का समर्थन करती है और क्लिनिकल विकास को अधिक कुशल तथा मरीज-केंद्रित बनाने पर ध्यान देती है।
Senior Bilingual Clinical Research Associate (French/English) – Canada Remote
Parexel is hiring a senior bilingual Clinical Research Associate to monitor clinical trials across Canada. The role manages site relationships, compliance, data quality, and study execution from site identification through close-out.
विवरण
- Conduct site qualification, initiation, monitoring, and termination visits at assigned clinical sites
- Prepare visit and contact reports
- Serve as the primary contact for building and maintaining clinical site relationships
- Investigate and resolve site questions and operational issues
- Protect study integrity and oversee site delivery from identification through close-out
- Assess trial performance and protect human-subject rights and well-being in line with study protocols
- Partner with clinical sites to create patient recruitment strategies that support enrollment timelines
- Maintain compliance with SOPs, protocols and amendments, GCP, and applicable regulatory requirements
- Assess reported-data quality and integrity, site performance, and investigational drug accountability
- Track the completeness and quality of regulatory documentation
- Verify site documentation
आवश्यकताएँ
- At least 18 months of direct on-site monitoring experience as a Clinical Research Associate (CRA)
- Bachelor’s degree or equivalent in biological science, pharmacy, or another health-related field
- Strong interpersonal, written, and verbal communication skills for working within a matrixed team
- Ability to work independently, act with urgency, and operate with limited supervision
- Client-oriented mindset with flexibility toward assignments and continued learning
- Ability to prioritize multiple tasks, assess changing situations, meet project timelines, and apply study-protocol knowledge
- Consistently honest and ethical approach to work
- Strong computer proficiency, including Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Excel, and Microsoft Word
- Fluent written and spoken English and French
लाभ
- Eligibility for a bonus incentive program
- Reduced travel and protocol workload compared with industry peers
- Access to advanced workplace technology
- Training tailored to individual experience
- Exposure to multiple therapeutic areas
- Opportunities for career advancement
- Ongoing career development through regular performance discussions and evaluations