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Title : AXA- Project Manager - R&D III -083
State : Connecticut   Date : Feb 6, 2019
Experience Level :  
Position Type : Project Manager - R&D III      
Description

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:New Haven, CT


Job Title: Project Manager - R&D III


Duration:  12+ months (extendable) contract on W2


Duties:




Drug Development Project Manager The Project Manager must generally be steeped in the business of drug development with the ability to take on work from our team and advance agreed deliverables with a high degree of independence. They must be comfortable working with teams and articulate both verbally and in written communications. MSProject is the key medium by which we develop timelines and any candidate we consider will be perfectly comfortable with this tool. We would expect this PM to be able to help team members see and understand how their activities contribute to the overall plan.



Skills:



Expertise in MSProject, Excel, Outlook, PowerPoint and general file management. High proficiency with Microsoft Project – timeline creation and modification, scenario planning, creation of timeline graphics w/One Pager Pro add-on. Technical proficiency with Project Web App (PWA) required. Expertise in Drug development – first-hand knowledge of activities associated with various stages of drug development. Ability to run/manage cross functional meetings with teams and individual team members to discuss activities, actions, timelines, and risks. Ability to work with teams to record meeting minutes and track action items. Ability to work with a team to update expense forecasts. Strong communication skills and ability to work with others. Minimum 10 years of experience in drug development/pharmaceutical industry Placing PM roles in two key areas Submissions. Cross functional submissions team support. Deep experience and expertise in successful medicine regulatory submissions in the US (minimum) including the ability to create an MSProject timeline to support such submissions. Ability to build a detailed submissions timeline with the team and organize document reviews that align with the timeline to accomplish filing deliverables External Innovation. Expertise in developing traditional and innovative strategies to pursue collaborations with external partners. We may acquire, co-develop and/or invest in new clinical stage assets that enhance our portfolio and exposure to new innovation , resulting in tighter integration of internal R&D efforts with BD. Develop agile and robust processes to identify, evaluate, access and integrate external opportunities. Assemble an overall R&D-BD playbook for the evaluation and potential integration of external opportunities




Education:



Bachelor's Degree



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Many Thanks,   

Sree Kanth
Recruitment Manager
Sree@newageclinical.com

NewAgeSys, Inc.
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