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| Employer Name: BiotechCrossing |
SpiderID: 2212528 |
| Location: Raleigh, North Carolina |
Date Posted: 5/3/2008 |
| Wage: |
Category: Biotech |
| Job Code: |
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Job Description:
Ensures the study is progressing according to internal and Customer quality standards, SOPs, GCPs and ICH guidelines to fulfill all federal and local regulations. 2. Serves as the team leader for the project team. Facilitates team building and communication. Acts as a liaison and facilitator between other departments within INCR and DataSpectrum for project related tasks and/or issues. Plans and projects resources required across all areas for studies. 3. Actively manages and mentors other Project Management staff (which may include: Senior Project Managers, Project Managers and Project Research Associates) in general team leadership skills, project management skills, internal INCR processes, and for project specific tasks. May work with the Project Manager on the study start up tasks (as the study start up expert) of a project to ensure success of the overall project. 4. Manages multiple projects ranging in size and complexity from single service studies to large full scope, multiple protocol projects, global projects and/or programs, with minimal interaction from supervisor. This includes management of resources, tasks, risk and quality.. 5. Manages the executed contract and financial aspects of assigned projects/programs. Reviews and approves study budgets and expenses and ensures all study related contractual and budgeting issues are upheld and performed. Oversees and tracks site payment issues as required. Ensures customers are invoiced in a timely manner and follows up on receipt of payment. 6. Develops knowledge of current therapeutic environment and drug development trends as needed. Facilitates team training in accordance with protocol and/or project requirements including therapeutic, protocol specific, and process training. May review protocol to ensure sponsorà €™s objectives are met and are in line with their Drug Development Program. 7. Reviews protocol, CRF and edit specifications for consistency within each document, and cross-checks these documents against each other.
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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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Web Site: http://www.biotechcrossing.com
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