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Job Title : Clinical Research Associate (CRA) II / Senior CRA.Must Have : Minimum 2 Years of On Site Monitoring Experience & 1 Year of Oncology Experience.
Our client is a global leader in healthcare da...Voir plusDernière mise à jour : il y a 4 jours
Please note this is an onsite position - eligible candidates must be able to reliably commute to Vittoria, ON for this position.
With the continued growth in the industry, Scotlynn is currently hiri...Voir plusDernière mise à jour : il y a 7 jours
Our client a leading heavy civils and structures main contractor is currently recruiting for a Site Superintendent to add to the team in Ontario.
The project is a involves looking after all Heavy, C...Voir plusDernière mise à jour : il y a plus de 30 jours
How many companies can say they’ve been in business for over 177 years?!.Here at ZEISS, we certainlycan! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced worl...Voir plusDernière mise à jour : il y a plus de 30 jours
Reporting to the Assistant Manager, Maintenance Operations, the Maintenance Site Supervisor role assists with daily coordination of the maintenance operations for 14 residence buildings on the Keel...Voir plusDernière mise à jour : il y a plus de 30 jours
Northwest Territories, accepting resumes from NT, NU, AB, BC, SK, MB, ON.Tundra Site Services is currently accepting resumes from.
This shift isnt yet confirmed, but interested candidates should sen...Voir plusDernière mise à jour : il y a plus de 30 jours
Heures de travail : 40 to 50 hours per week.Private sector land surveying establishments.Relocation costs covered by employer.
Develop survey plans, methods and procedures for conducting legal survey...Voir plusDernière mise à jour : il y a 6 jours
This is a Drive in / Drive out ONLY position.We are looking for a licensed industrial electrician with at least 2 years of underground experience for an exciting opportunity on an active producing mi...Voir plusDernière mise à jour : il y a 7 jours
Site Supervisor – Sewer & Watermain.Supporting the Project Manager, the Site Supervisor role supervises and oversees construction projects from start to finish.
They provide direction and guidance t...Voir plusDernière mise à jour : il y a 7 jours
Who We Are; What We Do; Where We’re Going.Magnet Forensics is a global leader in the development of digital investigative software that acquires, analyzes, and shares evidence from computers, smart...Voir plusDernière mise à jour : il y a plus de 30 jours
When our values align, there's no limit to what we can achieve.Bilingual- English / French proficiency.The Site Monitor will be responsible for data integrity, data quality and ensuring compliance wi...Voir plusDernière mise à jour : il y a 7 jours
At ACDF Architecture, we are recognized for our high level of expertise in building designs as well as for the technical quality of our achievements.
The firm is renowned in Quebec, Canada and inter...Voir plusDernière mise à jour : il y a plus de 30 jours
The Site Reliability Engineer will play a critical part in ensuring the reliability, supportability, scalability, and performance of our.
NET stack applications built with ASP.Partner with developer...Voir plusDernière mise à jour : il y a 6 jours
About Dokainish & Company Since 2011 Dokainish & Company has been providing world class professional consultancy services.
We specialize in working diligently and collaboratively with ...Voir plusDernière mise à jour : il y a 22 jours
The Remote Site Technicians will safely and effectively diagnose, repair and or assemble all Caterpillar mining and earthmoving equipment in a timely manner while ensuring high quality standards an...Voir plusDernière mise à jour : il y a plus de 30 jours
Reporting to the East Area Manager or Canadian Operations Manager, this position leads key aspects of site operations with responsibilities for ensuring financial and operational goals (safety, qua...Voir plusDernière mise à jour : il y a plus de 30 jours
Nurse Practitioner (NP) Flexible Assignments | Virtual & On-Site Options.Full-Time & Part-Time | Competitive Pay | Immediate Start | $110,000 to $117,000 annually.Join HealthOPM Empowering ...Voir plusDernière mise à jour : il y a 20 jours
Risk based monitoring is required • •.Conduct on-site and remote monitoring visits per the Monitoring Plan.Perform Source Data Review (SDR), Source Data Verification (SDV), and Case Report Form (CRF)...Voir plusDernière mise à jour : il y a 7 jours
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Clinical Research Associate (CRA) II / Senior CRA
i-Pharm ConsultingOntario, CanadaIl y a 4 jours
Type de contrat
- Temps plein
- CDI
Description de posteA minimum of 2 years of experience as a Clinical Research Associate (CRA) in a clinical research environment. At least 1 year of experience in oncology clinical trials, with a solid understanding of oncology treatment modalities and protocols. In-depth knowledge of ICH-GCP, FDA, and other regulatory standards and guidelines. Excellent organizational, communication, and problem-solving skills. Ability to travel to clinical sites as required by the study. A bachelor’s degree in Life Sciences or a related field (or equivalent experience). CRA certification (e.g., ACRP or SOCRA) preferred but not required.
Job Title : Clinical Research Associate (CRA) II / Senior CRA
Job Type : Permanent Full Time
Location : Canada
Must Have : Minimum 2 Years of On Site Monitoring Experience & 1 Year of Oncology Experience
Our client is a global leader in healthcare data, technology, and advanced analytics, dedicated to supporting the pharmaceutical and biotechnology industries in the development of ground-breaking treatments. With a strong focus on oncology, our mission is to accelerate the discovery and development of life-changing therapies. They are seeking a highly skilled Clinical Research Associate II (CRA II) to join our team and contribute to the success of cutting-edge oncology clinical trials.
Key Responsibilities :
- Oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to the study protocol, ICH-GCP, and local regulatory requirements.
- Conduct site initiation, monitoring, and close-out visits, offering continuous support to ensure optimal site performance.
- Establish and maintain strong working relationships with investigators, site staff, and other key stakeholders.
- Ensure accurate and timely collection and reporting of clinical trial data.
- Proactively identify potential risks and work with the study team to resolve issues affecting timelines, data quality, or compliance.
- Provide guidance to junior CRAs and assist in their professional development.
- Ensure all clinical trial documentation is maintained in compliance with regulatory requirements and company SOPs.
- Regional travel.
Qualifications :
If you are interested in finding out more about this role or others, please contact Sharleney Chandraratna at schandraratna@i-pharmconsulting.com or call : +44 (0) 2075510732