Biomedical Research Coordinator
15 hours ago
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
- 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.
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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