Clinical Trials Specialist

6 hours ago


Vancouver, British Columbia, Canada i-Pharm Consulting Full time

Discover a challenging and rewarding career as a Clinical Trials Specialist with i-Pharm Consulting, a global leader in healthcare data, technology, and advanced analytics.

We are seeking a highly skilled and experienced Clinical Research Associate II (CRA II) to join our team and contribute to the success of cutting-edge oncology clinical trials.

About the Role:

The successful candidate will oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to the study protocol, ICH-GCP, and local regulatory requirements. Key responsibilities include conducting site initiation, monitoring, and close-out visits, establishing strong working relationships with investigators, site staff, and other key stakeholders, and ensuring accurate and timely collection and reporting of clinical trial data.

A minimum of 2 years of experience as a Clinical Research Associate (CRA) in a clinical research environment is required, along with at least 1 year of experience in oncology clinical trials. In-depth knowledge of ICH-GCP, FDA, and other regulatory standards and guidelines is also essential. Excellent organizational, communication, and problem-solving skills are necessary for this role.

Salary & Benefits:

We offer an attractive salary package ranging from $120,000 to $150,000 per annum, depending on experience, plus additional benefits including health insurance, retirement plan, and opportunities for professional development.

Key Responsibilities:
  • Manage clinical trials at investigational sites, ensuring compliance with study protocol, ICH-GCP, and local regulatory requirements
  • Conduct site initiation, monitoring, and close-out visits
  • 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
Qualifications:
  • Bachelor's degree in Life Sciences or a related field
  • Minimum 2 years of experience as a Clinical Research Associate (CRA)
  • At least 1 year of experience in oncology clinical trials
  • In-depth knowledge of ICH-GCP, FDA, and other regulatory standards and guidelines

i-Pharm Consulting is committed to supporting the pharmaceutical and biotechnology industries in the development of life-changing treatments. If you are passionate about clinical research and have the required skills and experience, we would love to hear from you.



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