Biomedical Research Coordinator

15 hours ago


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

We are a global leader in healthcare data, technology, and advanced analytics, dedicated to supporting the pharmaceutical and biotechnology industries in the development of groundbreaking treatments. With a strong focus on oncology, our mission is to accelerate the discovery and development of life-changing therapies.



Job Overview

As an Oncology Clinical Trials Specialist at i-Pharm Consulting, you will oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to the study protocol, ICH-GCP, and local regulatory requirements.



Responsibilities
  1. Conduct site initiation, monitoring, and close-out visits, offering continuous support to ensure optimal site performance.
  2. Establish and maintain strong working relationships with investigators, site staff, and other key stakeholders.
  3. Ensure accurate and timely collection and reporting of clinical trial data.
  4. Proactively identify potential risks and work with the study team to resolve issues affecting timelines, data quality, or compliance.


Requirements
  • 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.


What We Offer

Our competitive salary for this role is $65,000 - $80,000 per annum, depending on experience.



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