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| Job #02377 |
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| About our client |
| Our client is the biotech division of a world-leading healthcare company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate! |
| Position |
Location |
| Clinical Research Associate – III |
Thousand Oaks, California |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Manage site selection 2) Conduct study site monitoring visits (qualification, initiation, interim and closeout) 3) Prepare reports in a timely manner in accordance with the monitoring plan and SOPs 4) Collect/review documents from sites, including site informed consents 5) Drive site budget and negotiate with sites 6) Assist in the development of monitoring plan and CRFs 7) Manage vendors and vendor set-up 8) Mentor junior CRAs 9) Participate in and present at Investigator meetings |
| Requirements |
1) Bachelor’s degree in a scientific discipline 2) 3+ years of field monitoring experience in the pharmaceutical or biotech industry, from qualification to closeout 3) Experience in mentoring junior CRAs 4) Strong knowledge and understanding of FDA Regulations and GCPs 5) Ability to set up and manage vendors 6) Exceptional communication skills 7) Willingness to travel – up to 75% |

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