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Senior Manager, Clinical Projects Job
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| Employer Name: BiotechCrossing |
SpiderID: 2196191 |
| Location: King of Prussia, Pennsylvania |
Date Posted: 4/19/2008 |
| Wage: |
Category: Biotech |
| Job Code: |
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Job Description:
Works closely with Marketing, Medical Affairs, Commercial Operations, Clinical Research & Development, Regulatory and others to develop preliminary study concepts into more detailed study proposals. Coordinates the internal review process for assigned study proposals, Once a proposal is approved, coordinates development of full protocol., CRFs, ICFs and other trials documents as well as a final study budget in concert with CROs and/or other internal and external team resources. Oversees and manages day-to-day activities and tasks performed by the study team to ensure assigned projects meet quality, budget and timeline specifications. Tracks and supervises project process, identifying and evaluating project risks throughout the project cycle implementing corrective action as appropriate. Responsible for identifying, qualifying, contracting and managing external vendors as appropriate to perform/conduct project related tasks or functions that are not preformed within company. 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.
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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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