Associate Director, Clinical Trials job Westminster Colorado
Associate Director, Clinical Trials job Westminster Colorado
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Associate Director, Clinical Trials Job


Employer Name: BiotechCrossing SpiderID: 2298696
Location: Westminster, Colorado Date Posted: 6/20/2008
Wage: Category: Biotech
Job Code: 5300234

Job Description:


This position reports to the Sr. Director of Clinical Trials. Provides leadership and expertise for the successful execution and management of Phase 2-4 international cardiovascular clinical trials. Manages study teams to ensure deployment of resources. Responsible for oversight and strategic direction and implementation across a number of studies to ensure clinical programs are conducted to meet project milestones and budgets through close partnership with parties involved both inside and outside of the company. Clinical Trial Management representative on Project Leadership Teams and other committees within Clinical Trial Management to assure best practices. Contributes to development of clinical and regulatory documents across the clinical development and regulatory submission lifecycles. Represents the company at external meetings. Assists the Senior Director in resource planning and staff training. Other responsibilites as directed. Requirements Essential Duties and Job Functions: Requirements include extensive experience in managing clinical trials; excellent verbal, written, and interpersonal communication skills; demonstrated ability to participate in and lead multifunctional teams, manage staff, and mentor junior staff; detailed understanding of pharmaceutical regulatory requirements and impact on development of clinical trials. The candidate must be able to solve complex problems and use highly developed independent judgment relating to regulations, guidelines, investigator interactions, vendor relationships, budgets, and timelines. Experience as a Clinical Trial Manager or Clinical Program Manager in the pharmaceutical or CRO industries required and experience in managing teams of direct reports required. Experience in oversight of large multi-study programs and in cardiovascular clinical research experience preferred. Knowledge, Experience and Skills: Typically requires a bachelors degree in biological sciences or healthcare, or relevant scientific discipline. Clinical research background and 8 to 10 years relevant clinical research experience is required. Previous experience as a Clinical Trial or Clinical Program Manager in the pharmaceutical industry is required. Cardiovascular clinical or clinical research experience is highly preferred.

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
City: Pasadena
State: California
Zip: 91101
Web Site: http://www.biotechcrossing.com

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