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Title : NVG- Project Coordinator -886
State : California   Date : Oct 22, 2020
Experience Level :  
Position Type : Project Coordinator      
This position is for a leading pharmaceutical company. Below are the details of the engagement. If you are available and interested please send me your updated word resume & your expected hourly rate on W2 ASAP.
Looking forward to hearing from you soon.

Work Location: Carlsbad, CA

Job Title: Project Coordinator

Duration: 12+ months (extendable) contract on W2


Works in a GMP/GCP/GLP/CLIA regulated environment and is responsible for following all applicable regulations 
Learn and be familiar with current laboratory offerings/capabilities 
Support lead project manager with running ongoing clinical trials: 
Monitor and update project deliverables including specimen shipments and clinical trial testing 
Document problem/occurrence logs; work with investigator sites and project teams to resolve open issues 
Track specimen accessioning, testing and reporting 
Manage specimen inventory for shipments and testing 
Identify potential specimen/testing issues; escalate critical problems to supervisor 
Assists with drafting of internal study-specific documentation 
Assists with development of study-specific training documentation 
Prepare agenda & minutes for internal project meetings 
Keep metrics to evaluate project goals and review trends 

Other Responsibilities: 

Ensuring that Quality Events such as incidents and deviations are proper documented, and for supporting/owning the immediate remediation and preventative actions 
Ensuring change requests are properly initiated, completed, and approved prior to the use of the assay, system, instrument, software, etc. being changed 
Maintaining up-to-date training records and ensuring training is complete prior to performing specific job functions 
Following approved and effective procedures to perform specific job functions, and ensuring procedures accurately reflect activities being performed.


Demonstrated strong customer and service focus. 
Excellent written, verbal and interpersonal communication skills, including the demonstrated ability to work in a team setting and foster collaborations – both internally and externally. 
Demonstrated ability to be flexible and adaptable to changing business needs. 
Strong organizational skills 
Knowledge of logistics and clinical trial operations a plus. 
0 – 2 years related project coordinator experience in a relevant industry, preferred.


Bachelor’s degree 
Related Project Management coursework and/or experience desired.

Many Thanks,   

Sree Kanth
Recruitment Manager

NewAgeSys, Inc.
Direct: 609-945-1736 Fax: 609-228-4079
600 Alexander Rd, Suite 3-3 
Princeton , NJ 08540 
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