Job Description

My client is a small biopharma who are currently in a growth stage. They are looking for a Senior CRA who is a specialist in CNS - Pain Studies, to help them achieve their goals.

Do not hesitate to apply, this is an urgent need and this opportunity will not be around for long.

This is a high travelling, on-site monitoring contract Clinical Research Associate opportunity for a West-Coast based Contractor. Pharma and Biotech experience is a must, Pain Management study experience is also a must! Spine studies experience is also highly desired. Multiple sites to manage across the West Coast, all monitoring will be on-site.

Responsibilities:

• All monitoring is on-site.
• Assess monitoring visit reports and identifying or communicating trends.
• Support CDM activities by completing data query and data review.
• Ensure documents are complete and in line with GCP/ICH and any other applicable regulatory demands.
• Add to the development of clinical protocols and relevant clinical forms.
• Build and execute a plan to deal with any backlogs.
• Develop a project management plan, project budget and study templates and study relevant tools required for the study
• Assess monitoring visit reports and identifying or communicating trends to management.

Desired Background:

• 10+ years of experience as a Clinical Research Associate.
• 3+ years of recent experience in CNS - Pain
• A life science bachelor’s degree.
• knowledge of clinical trial regulations such as GCP/ICH and FDA requirements.
• Open to high levels of travel.

If you are interested, get in touch with me ASAP by simply applying below.

You can also send your most up to date CV directly to me, and I will reach out to you.

JDMandarin@barringtonjames.com

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