10+ years of clinical research experience from pharma, biotech or CRO background
Study management experience
CRO/vendor management/oversight experience
Develop and monitor metrics to evaluate the monitor and site performance
In-house Lead CRA, San Diego, Biotech, onsite contract assignment (long term) 50/50 travel/office An exciting biotech company in Southern California who have multiple drugs commercialised and a have several more studies in phase II-III are actively recruiting for an in-house, Lead CRA to join a busy Clinical Operations team on a long-term assignment that will require the individual to be onsite and work 40 hours per week. This will likely be 50% travel to clinical sites; 50% working from the office in San Diego. You will meet the following requirements: 10+ years of clinical research experience from pharma, biotech or CRO backgroundStudy management experienceCRO/vendor management/oversight experienceDevelop and monitor metrics to evaluate the monitor and site performance. In the event of performance concerns, evaluate cause and mitigate risk to study.If you are interested in this role and meet the above requirements, please apply immediately with your latest resume for instant consideration.Key Words: Senior, Sr, Snr, Lead, CRA, Clinical, Research, Associate, Biotech, Pharmaceuticals, CRO, San, Diego, CA, California, Travel, In-House, Study, Management, Vendor, Oversight, QC, Management, Monitor, Monitoring
Clinical Study Risk Manager
Senior CRA DACH Region – Rapidly Growing Small Pharma – Global Hub Basel
10+ years’ experience in clinical research, working in pharmaceutical/biotech industries
Demonstration of solid progression into clinical operations senior-level role
Recently experience of managing oncology trials
Vendor/CRO oversight and QC experience
A leader in clinical operations and clinical research recruitment, we place professionals in more than 50 countries.
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