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| Company: |
Sterling Life Sciences |
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| Job Title: |
Project Manager |
| Job Category: |
Biotech |
| Job Location: |
San Diego - CA California - USA |
| Job Ref. Number for your records: |
2440 |
| Job Description: |
Job Responsibilities:
1) Manage the day-to-day strategic and tactical aspects of multiple or large-scale projects
2) Oversee clinical project managers working on projects within development programs
3) Review high-level deliverables across projects and oversees project gating, resourcing and coordination
4) Work closely with Development Teams to ensure empowerment and team performance
5) Anticipate and identify project schedule slips or changes and analyzes scope, cost and resource impacts
6) Facilitate development and execution of project change management
7) Develop and maintain effective ongoing relationships with strategic partners (e.g. CROs)
8) Manage scope and mitigates risk across projects
9) Ensure accurate vendor invoicing, and monitors expenses for all projects under his/her direction
10) Analyze project earned value for multiple projects
11) Address expense or invoicing issues when they arise
12) Communicate effectively relevant project information to superiors and peers
13) Work across projects and development programs to share lessons learned and best practices
14) Assess project management training needs and selects training tools for team members
Job Requirements:
1) Bachelor’s degree within a health/biomedical sciences field, or related field and equivalent experience
2) Advanced degree (preferred)
3) Project Manager Certification (preferred)
4) Minimum 5-7 years of experience specifically within Project Management in the pharmaceutical/CRO industry
5) Strong critical thinking and clinical skills are essential
6) Strong ability to prioritize and organize workflow activities in a fast-paced environment
7) Proficient in basic computer programs – MS Office Suite and MS Project
8) Excellent communication skills; ability to tactfully communicate sensitive information
9) Ability to work independently and in a cross-functional team environment
10) Extensive understanding of clinical development, regulatory and QA, CMC, clinical trials operations and project management methodology
11) Demonstrate ability to assist in the evaluation and redesign of project management methodologies
12) Awareness of new and emerging project management methodologies and technologies, including Best Practices, and the potential application on development programs
13) Willingness to travel – 20-25%
Applicants are encouraged to apply directly by going to: Sterling Life Sciences job board
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| Skills Required: |
Strong critical thinking and clinical skills are essential
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| Language Requirements: |
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| Employment Type: |
Full Time
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| Yearly Salary: |
115 USD
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| Posting Date: |
Oct 19 2007 |
| Education level required: |
Bachelor
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| Experience (in years): |
3 to 5 Years |
| Company: |
Sterling Life Sciences |
| Contact Name: |
Sterling Life Sciences |
| Preferred Method of Contact: |
No Preference |
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