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CLINICAL TRIALS MANAGER

GlobalChannelManagementInc

Raritan, NJ, United States contract

Posted: January 19, 2017

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Quick Summary

We are seeking a Clinical Trials Manager to join our team in Raritan, NJ, to oversee the day-to-day operations of our global channel management business. The ideal candidate will have a strong background in clinical trials management and a passion for working with diverse teams to deliver high-quality results. The successful candidate will be responsible for managing a team of account managers and recruiters, developing and implementing strategies to reduce training and labor costs while ensuring the best talent is brought to the organization.

Job Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

 

• Bachelor Degree required, preferably in biological or medical sciences.  Master's Degree or higher is desirable.  
• Minimum
of 8 years direct clinical research experience, of which a minimum of 4
years clinical research supervisory or management capacity with
budgetary responsibility.
• Knowledge of applicable standards and regulations for clinical trial and laboratory conduct
• Proven oral and written communication skills
• Proven planning skills; ability to create and track detailed project plans
• Proven interpersonal, leadership and organizational skills & Effective time management
• Ability
to work independently and within a cross-functional team environment to
analyze and solve problems, and to make sound decisions
• Basic biostatistical knowledge
• Must
be willing to periodically work with potentially biohazardous materials
in an approved safe manner and to work in biohazardous environments
• Demonstrated experience in computer skills to include Microsoft Word, Excel and basic templates

Preferred:

• 2 years IVD Monitoring experience
• Experience in Cardiac clinical studies
• Strong technical lab expertise with demonstrated ability in assay analysis and data interpretation

$44/hr

12 months

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