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Clinical Research Associate Job
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| Employer Name: |
SpiderID: 2400238 |
| Location: Los Angeles, California |
Date Posted: 7/28/2008 |
| Wage: 72,000-90,000 |
Category: Medical/Health |
| Job Code: CRA |
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| Number Of Openings: 5 |
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Job Description:
Clinical Research Associate
Salary Range: 72 – 90,000 USA
Clinical Research Associates will carry out activities that may include investigational site selection, set up, initiation, monitoring and close-out as required by the Sponsor, whilst working to ICH-GCP, local regulations and company and/or Sponsor SOPs with appropriate levels of supervision and support.
Study Start-Up
• To conduct site selection visits.
• To co-ordinate essential documents for sites and investigators.
• To plan, coordinate, and conduct site initiation visits.
• To ensure that all contact (including written reports and follow up letters) generated for all aspects of the the pre-study and initiation contacts with investigators.
Monitoring
• To plan, coordinate, and conduct monitoring visits.
• To provide ongoing training of the site personnel regarding trial specific information and updates to industry standards.
• To collect data from clinical sites and work with Data Management to ensure timely resolution of data queries in order to achieve project deadlines.
• To ensure that supplies of study materials are maintained at designated sites .
• To ensure subject safety issues are identified and all Serious Adverse Events are reported. • To ensure all project tracking systems are maintained in order to track clinical trial subjects and data collection/review status within the clinical trial.
• To ensure ongoing reporting requirements for regulatory, ethical and local bodies are met for designated sites.
Study Close-Out
• To conduct close-out visits and collect all data and supplies from sites..
Job Requirements:
Requirements:
BSc in life science related field OR Registered Nurse is acceptable.
• Good organizational skills
• Excellent communication and interpersonal skills
• Good administrative and writing skills
• IT skills (e.g., Microsoft Office platform)
• Good knowledge of clinical research and clinical trial material development industry
• Proven experience of monitoring clinical trials to regulatory standards (i.e., ICH GCP)
Job Criteria:
Start Date: Aug. 20,08
Position Type: Full-Time Permanent
Years of Experience Required: Entry-Level
Education Required: Bachelors
Overnight Travel: 50-75%
Vacation Time: Negotiable / Other
Contact Information:
| Contact Name: Alex Dzyubenko |
Company Type: |
| Company: |
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| City: New York |
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| State: New York |
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| Zip: 10022 |
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Web Site: http://www.espoirbridge.com
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