Clinical Research Associate / Senior
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Location
California
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Sector:
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Salary:
Negotiable
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Contact:
Chris Brough
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Contact email:
Chris.Brough@volt.eu.com
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Job ref:
BBBH1515_1627658952
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Published:
over 2 years ago
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Expiry date:
2021-09-28
Key Requirements:
Conducting site visits, including pre-study, initiation, monitoring and close-out
Adherence to all FDA, ICH-GCP and local regulations
Ensuring the accurate completion and collection of regulatory documents
Performing data verification
Ensuring implementation and compliance with FDA, ICH-GCP guidelines
Participating in budget negotiation and follow-up where applicable
Assisting with data validation and query resolution
Mentoring junior team members in their development.
Qualifications:
A minimum of 2 years of monitoring experience in oncology trials
In Depth level of oncology knowledge
Science=Related Bachelor's degree
Excellent knowledge of clinical monitoring process
Expert ICH-GCPs knowledge
Experience with clinical trial information systems & various eTMF
Ability to travel up to 60% on average