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Associate Director, Clinical Research Oncology Job
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| Employer Name: ClinicalresearchCrossing |
SpiderID: 2350815 |
| Location: Ridgefield, Connecticut |
Date Posted: 7/8/2008 |
| Wage: |
Category: Miscellaneous |
| Job Code: 6229789 |
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Job Description:
Must have thorough medical/scientific knowledge of the therapeutic area, analytical skills, knowledge of drug development and regulatory requirements. Excellent interpersonal verbal/written communication skills. Ability to work as part of a team. DUTIES AND RESPONSIBILITIES: Responsible for the conduct/management of clinical trials including protocol development, study conduct and reporting. May include assignment as Trial Clinical Monitor, Local Clinical Monitor or both for one or more trials. Also responsible for providing input on medical issues. Supervise the appropriate clinical staff in their execution of operational aspects of clinical trials/projects. Responsible for the interpretation and summarization of clinical data and for documenting such information in the medical sections of regulatory documents such as the IND, IND annual reports, Clinical Trial Reports, NDA, and NDA annual reports. Provides medical judgement on safety sections. May also review labeling for marketed drugs, manuscripts, publication plans and press releases. Responsible for assuring adherence to governmental regulations and guidelines and BI SOPs in the preparation, conduct and reporting of clinical trials.
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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: ClinicalresearchCrossing |
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| City: Pasadena |
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| State: California |
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| Zip: |
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Web Site: http://www.clinicalresearchcrossing.com
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