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Clinical Program Manager Job
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| Employer Name: BiotechCrossing |
SpiderID: 2246194 |
| Location: Tarrytown, Ohio |
Date Posted: 5/30/2008 |
| Wage: |
Category: Biotech |
| Job Code: 5072666 |
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Job Description:
Oversee and manage all activities related to the conduct of clinical research projects in order to meet deliverables and program objectives. Interacts with various internal and external vendors as well as clinical study sites. Periodically travels to assure compliance with protocol and clinical research project objectives. Responsibilities includes, Performs job duties with minimal guidance. Delivers high quality program deliverables on time and within budget Manages, tracks, and troubleshoots a series of related trials within a single program Identifies program risks; proactively creates and implements mitigation strategies Has operational expertise and communicates effectively operational needs to ensure goals are met Keeps apprised of all decisions in order to ensure established goals are attainable prior to the consensus to implement Develops work plans, establishes clinical research objectives, assigns tasks and supervises Clinical Trial Managers Maintains schedules (timelines) for overseeing assigned clinical research studies and facilitates decision making in order to adhere to timelines Provides guidance to Clinical Team by establishing clinical research goals that are aligned with established policies and standards for the department and organization Identifies and recommends changes to established practices and policies which affect subordinate resources. Working knowledge of clinical research database systems. Must be able to develop and present varied and unique ideas. Develops and provides challenging yet appropriate assignments and communicates progress toward development goals. Strong leadership skills; communicates and demonstrates vision and commitment. Effective influence and relationship management skills Financial acumen in creating and managing clinical program budget Builds successful collaborations with internal and external partners Strong communication skills; verbal, written, and presentation Broad knowledge and cross-functional understanding of clinical trial methodology Knowledge of GCP and ICH. Directs and coordinates the operation of a program of sufficient size to require the use of subordinate supervisors. Bachelors degree (B.S.) in the Life Sciences Discipline from a four-year college or university (advanced degree preferred), minimum seven (7) years of clinical research experience in the Pharmaceutical industry, preferably in multiple phases, as well as minimum 2 years management experience.
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For further information, please visit us online at http://www.biotechcrossing.com
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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: BiotechCrossing |
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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.biotechcrossing.com
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