Clinical Program Manager Job

Employer Name: PharmaceuticalCrossing	SpiderID: 2326524
Location: Cambridge, Massachusetts	Date Posted: 6/30/2008
Wage:	Category: Medical/Health
Job Code:

Job Description:
Authors and/or reviews clinical content of protocols * Authors, reviews and approves informed consent documents per Seaside SOPs * Presents at investigator meetings * Tracks study progress, including regulatory document collection, IRB approval and enrollment * Manages field-based Clinical Research Associates (CRAs) * Reviews case report form data for safety and efficacy parameters * Provides input into clinical study reports Job Qualifications * B.S. degree with a minimum of 5 years of clinical research experience in the pharmaceutical/biotechnology industry or within a Clinical Research Organization * Clinical study management experience, including CRA management * Thorough knowledge of the clinical research process, FDA regulatory requirements as well as ICH and GCP Guidelines * Effective oral and written communications skills * Ability to constructively problem solve while dealing with time constraints * Ability to manage and influence without direct authority * Ability to work both within a team and independently *

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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: PharmaceuticalCrossing

City: Pasadena
State: California
Zip:

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