Associate Director, Clinical Research Oncology Job

Employer Name: ClinicalresearchCrossing	SpiderID: 2384509
Location: Ridgefield, Connecticut	Date Posted: 7/21/2008
Wage:	Category: Miscellaneous
Job Code: 6229789

Job Description:
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. Also responsible for interpreting such guidelines to direct reports and investigators. Develops and maintains relationships internally with others involved in the drug development process, and externally with investigators, consultants and contract research organizations.

For more information, please click here to visit us at ClinicalresearchCrossing

For further information, please visit us online at http://www.clinicalresearchcrossing.com

Sign Up Now

Job Requirements:
6229789

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

City: Pasadena
State: California
Zip:

Web Site: http://www.clinicalresearchcrossing.com