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Project Manager Scrum Master

Ordinateur et Logiciels

215 jours | San Francisco, California, United States | CONSULTANT SPECIALISTS, INC. (CSI)

Project Manager Scrum Master

215 jours | San Francisco, California, United States | CONSULTANT SPECIALISTS, INC. (CSI)

CONSULTANT SPECIALISTS, INC. (CSI)

Date de début :septembre 16

Appliquer avant :octobre 17 2020

Industrie : Ordinateur et Logiciels,

Description du poste

W2 ONLY. No exceptions

Candidates who are located San Francisco Bay Area are ideal. If you are not local but want to be considered, for this role, you will need to take care of your re-location on your own.

Please email your resume attached as a Word Doc to Ellen through this website.

PM Clinical / Molecular Strategy

Project name: CRISP (Connecting Regulatory Insight & Policy)

Project vision is to build a knowledge management database related to molecule strategy.

PDR currently has strategy and insights regarding molecule strategy in various places such as ppt, gdoc, etc. When a new molecule is being developed, the scientists often have to rely on their network to procure data and information to help them design their molecule strategy.

A database will enable them to pull relevant data and learning from "precedents" when required, help them make better decisions and enable more efficient interactions with health authorities. They will build operational and analytical dashboards on top of the database.



Key skills required of the PM/Scrum master-

  1. Ability to partner with the business closely and contribute to project strategy, governance, and light OCM/training/adoption planning activities
  2. Ability to lead through ambiguity (at least initially)
  3. Agile mindset is important. He/she may not play an active scrum master role but will manage scrum masters and will be seen as an agile coach/influencer to the team
  4. Experience with vendor solution analysis/negotiation
  5. Experience running POCs
  6. Business and IT team members are primarily in SSF, but there is a small development team in Poland
  7. 50% allocation suffices at this time. It will ramp up to 100% as the POC comes to a close and it spins off into a project
  8. Knowledge of clinical and regulatory domain is a huge plus
  9. Experience working with IT Security, Privacy, Quality on SRAs, DCRs, Vendor assessments is important

Regulatory Experience in Healthcare

Pharma regulatory applications, data and processes

Required

  • DATA GOVERNANCE
  • AGILE PDM
  • PROJECT MANAGER
  • VENDOR NEGOTIATIONS

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