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Senior Manager, Clinical Projects Job
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| Employer Name: BiotechCrossing |
SpiderID: 2369211 |
| Location: King of Prussia, Pennsylvania |
Date Posted: 7/15/2008 |
| Wage: |
Category: Biotech |
| Job Code: 6313642 |
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Job Description:
Ensures that clear and manageable communication lines are established and maintained between the study team, vendors, management and other relevant stakeholders. Works with publications teams and other internal key stakeholders as well as KOLs, medical writers and other to product publications and abstract submissions to targeted national and international medical meetings. Performs resource planning and supports the study team to ensure adequate resourcing of assigned projects. Coordinates preparation and/or prepare project status reports to ensure management and other key stakeholders are kept informed of project progress and status. Conducts regular study team meetings ensuring minutes and action plans are prepared and circulated. Prepares and manages overall project budget for assigned project(s) taking overall responsibility for adherence to budget timelines and quality specifications. Manages project(s) assigned in accordance with Standard Operating Procedures. Serves as functional manager for one or potentially more other clinical trial managers. Represents the clinical research team as company processes are optimized and harmonized. Takes the lead in trouble-shooting operational issues that affect the clinical program and works to optimize the evolving process. Reviews and/or manages (contracts, budgets, proposals and communications) Investigator Initiated Trials/Trial proposals in cooperation with commercial departments. Performs other duties as assigned to meet departmental and company objectives. Qualifications: Training and Experience College degree, preferably MD or PhD Minimum 3 years of clinical research experience including four years of clinical study management experience in a pharmaceutical/biotechnology company, CRO or clinical trials research environment is required. Previous on-site clinical research experience (e.g. as a study coordinator or CRA) preferred. Previous matrix or line supervisory experience is desired.
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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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