Job Description

Reference # : 17-07397Title : Technical Project Manager (Pharmaceutical Experience Required)
Location : Groton, CT
Experience Level : Start Date / End Date : 09/25/2017 / 05/24/2018
Assignment Detail
Industry:Biotech/Pharma
Description
ECLARO is a company that delivers talent. We provide fully customizable, comprehensive talent acquisition and management of seasoned professionals through a number of business models, including: Consulting, Professional Hire, Global Integrated Delivery™ and Managed Services.

Technical Project Manager
Eclaro is looking for a Technical Project Manager for an 8 month contract opportunity for our client located in Groton, CT.

Job Description:
Key areas of support:
The project manager for this workstream will report in regularly to the program manager for the NEXTGEN PMO and Volume 2 workstream and will support the following:
  • Update the charter for the workstream for 2017
  • Portfolio assessment and management – review, prioritize and manage CDISC submission needs from 2017-2019
  • Portfolio assessment will assist with prioritization and/or finalization of SDTM specification work
  • Consider prioritization of standards for enterprise specification work and study conversion needs based on submission schedule
  • Consider prioritization of standards enterprise specification based on new study starts
  • Support study conversion –prioritize standards for development based on submission schedule and reporting requirements
  • CDARS (Pharmaceutical reporting system) CDISC/CaPS implementation – programming development and implementation plan based on priorities noted above
  • Work closely with the SGS Project Manager (Statistical Guidance Standards) and with Programming standards group to prioritize the development of end points definition to support priority reporting
  • Work directly with project teams to confirm project deliverables and timelines
  • Create and maintain a Project Plan based on reporting priorities
  • Communicate priorities to the CDISC PMO workstreams to align priorities
  • Weekly QUAD report updates to program manager as part of PMO deliverables
  • Escalation of any workstream issues to the PMO program manager.
Qualifications:
  • Strong PM skills (PNBOK/PMP certified or equivalent)
  • 5+ years of experience deploying IT/BT projects within the pharmaceutical industry
  • Understanding of standards management or CDISC knowledge desirable
  • Proficiency with Microsoft Office suite and Microsoft Project
If interested, you may contact:
Cheryl Buot
Cheryl.Buot@eclaro.com
(212) 901-3840
www.linkedin.com/in/cheryl-buot-56ba4836

ECLARO recruits and manages a staff of highly skilled individuals in an array of specialized disciplines. This approach enables our clients to leverage new opportunities, respond to increased and changing demands and increase their profitability. Please visit www.eclaroIT.com to see why the Right People are The Answer™.

Specialties: Customized solutions for Human Capital and Talent Acquisition, Permanent placement and retained search, Recruiting, Staff Augmentation, Contract Labor, Managed Services, RPO, MSP, VMS, IT solutions, management and support, offshore business process outsourcing.

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Website:
http://www.eclaro.com
Industry: Staffing and Recruiting
Type: Privately Held
Company Size: 501-1000 employees
Founded: 1999

Application Instructions

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