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Clinical Research Associate (CRA) II / Senior CRA

Clinical Research Associate (CRA) II / Senior CRA

i-Pharm ConsultingOntario, Canada
11 days ago
Job type
  • Full-time
  • Permanent
Job description

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 :

  • A 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.

    • If you are interested in finding out more about this role or others, please contact Sharleney Chandraratna at [email protected] or call : +44 (0) 2075510732

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