Senior Clinical Research Associate

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada: Conduct and report SIV, RMV, COV onsite monitoring visits Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Prepare and particiapte on audits and inspections Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience Experience in all types of monitoring visits in Phase II and/or III Experience in Oncology is a plus Full working proficiency in English and French. Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel Valid driver’s license Additional Information For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future. This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. Compensation: CAD 120000 - CAD 150000 - yearly

The Senior Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and manage site communications. They will also support regulatory document preparation and participate in study audits and inspections.

Candidates must hold a college or university degree in Life Sciences and possess independent on-site monitoring experience in Phase II or III trials. Proficiency in English and French is required, along with the ability to travel and a valid driver's license.

• Résolution de problèmesSouhaitée
• CommunicationSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical Research
• On-site Monitoring
• CRF Review
• Source Document Verification
• Query Resolution
• Site Management
• Regulatory Documentation
• Audit Preparation
• Inspection Support
• Feasibility Research
• Oncology
• MS Office
• Multitasking
• Problem-solving
• Communication
• Collaboration
• Support Services
• Research Support
• Bilingual (French/English)
• Valid Driver's License
• Auditing
• Medical Science
• Management
• Problem Solving
• Life Sciences
• Source Document

• Healthcare
• Science & Research
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Formation minimale

Baccalauréat

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine