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Clinical Trial Monitor
3 weeks ago
Monitoring Clinical Trials Role Available
We are currently seeking a seasoned professional to lead the monitoring of clinical trials. This role will be responsible for ensuring that projects are conducted in accordance with applicable SOPs, regulations and ICH guidelines.
- Key Responsibilities:
- Monitor clinical trials at sites and ensure compliance with project requirements.
- Collaborate with Project Managers to stay informed on all aspects of the project.
- Ensure timely and compliant maintenance of project documentation.
Requirements:
- Education: Undergraduate degree in Life Sciences (e.g., Biology, Chemistry, Pharmaceuticals).
- Experience: At least 3-4 years' experience in monitoring clinical trials in CRO, Pharmaceutical and/or Biotechnology industry as a SCRA/CRA.
- Skills: Experience in EDC & CTMS, site management from feasibility to site close-out, contracts negotiation desirable, HREC submission preparation.
- Personal Qualities: Understanding and practical knowledge of ICH-GCP requirements, willingness to travel.
Benefits:
- Opportunity to work on early phase oncology trials.
- Chance to develop skills in managing site-management processes.
