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Senior Director, Clinical Operations Job
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| Employer Name: BiotechCrossing |
SpiderID: 2192974 |
| Location: Cranbury, New Jersey |
Date Posted: 4/17/2008 |
| Wage: |
Category: Biotech |
| Job Code: |
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Job Description:
Support all therapeutic areas by overseeing all operational functions, with a focus on project and resource management for clinical activities Direct the management and maintain strong, effective relationships with vendors, consultants, investigators, and other external clinical trial participants Oversee internal and external budgets for clinical operations Support the development and implementation of standards, tools, and procedures to improve clinical research efficiency Ensure that clinical trials are conducted and reported in accordance with GCP/ICH, QC/QA, SOPs, and Company Best Practices Guidelines Assist with the generation, analysis, and presentation of clinical data Collaborate effectively with other groups in Clinical Research, as well as multidisciplinary project development teams (including R& D, Pre-Clinical Development, Regulatory Affairs, Program Management, Finance, Legal & Business Development) Provide appropriate training, mentoring and career development for staff Requirements Bachelors Degree or equivalent within a life science or health field is required Minimum of ten years of clinical trial experience in a pharmaceutical, biotech or CRO industrial setting, including significant experience managing clinical trials outside the US Minimum of five years supervisory experience, including responsibilities for organizational budget and staffing plans, and management of multiple levels of staff Demonstrated leadership abilities, including setting a vision for others and driving to achievement of objectives in accordance with allocated resources and timelines. Ability to plan and lead the growth of an evolving organization Demonstrated sense of urgency and ability to solve problems, work independently and under tight deadlines; strong work ethic and initiative Experience with conduct of investigational trials (Phases 1-3) in US, Europe and other countries Knowledge of all aspects of GCP and US and EU regulations governing investigational clinical trials and new product registration Expertise in cross-functional aspects of drug development; successful work in cross-functional (matrix) teams and project management.
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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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