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Clinical Trial Manager Job
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| Employer Name: BiotechCrossing |
SpiderID: 2366533 |
| Location: Durham, North Carolina |
Date Posted: 7/14/2008 |
| Wage: |
Category: Biotech |
| Job Code: 6205947 |
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Job Description:
Serve as supervisor for assigned Clinical Operations staff within therapeutic area(s) and assess assigned staff on work assignments, utilization and productivity. Develop written performance standards for Clinical Operations personnel. Conduct performance evaluations for assigned staff. Work with internal and external training resources as required, ensure that all staff assigned, are current with their required training (non-study specific) including SOPs, ICH/GCP, and field-based training. Therapeutic Area Support and Strategic Planning Coordinate the standardization and maintenance of status reports and other information sources. Facilitate communication with global partners and key therapeutic area investigators when issues arise that affect multiple projects and/or the entire Therapeutic Area. Work with the Project Leader to facilitate cross-functional team and multiple business-partner communication for proactive study-wide problem solving regarding study progress and trial issues. Assist with the coordination and prioritization of team efforts and assess overall project metrics and study timelines across the Therapeutic Area. In coordination with Project Leaders, identify and notify appropriate parties of emerging out of scope activities, project change orders and study guidelines. Evaluate impact on resource needs, study processes and related documents. Collaborate with clinical operations personnel to identify current and anticipate long-term staffing resource needs. New Business Development Collaborate with the Therapeutic Area management, proposal writing personnel, and the proposal project leader in the development of scope of work, associated budget and timelines for new business proposals as required. Participate in the development of the protocol, protocol revisions and amendments, monitoring plan, scope of work and operations manual as required. Provide input for the development of the CRF (data capture forms)
For more information, please click here to visit us at BiotechCrossing
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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