Job Description

Project Manager
Job Number: 21-01931
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Project Manager for our client in Lawrenceville, NJ. 
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Responsibilities:
  • Provides project management support to GDMCM leadership on assigned projects ensuring the same are completed on time and within budget, including:
    • Developing a project plan with key activities, dates, deliverables, and owners
    • Planning for, scheduling and facilitating project meetings
    • Preparing materials required for the meetings
    • Distributing meeting minutes and following up on action items
    • Ensuring issues are being resolved effectively
    • Keeping leadership informed of status
    • Ensuring appropriate stakeholder engagement on the projects and facilitating change management efforts
  • Additional responsibilities may include:
    • Creating metrics and reports as requested by the GDMCM leadership
    • Facilitating the process for updating GDMCM procedural documents, working with Client SMEs and Client Technical Writers to ensure the documents are updated correctly and on time
    • Managing and contributing to continuous improvement projects within the GDMCM organization
    • Facilitating database lock risk assessment meetings and database deployment/migration meetings and tracking the status of the locks and deployments
    • Creating slide materials for leadership meetings as requested
    • Developing and/or updating business process flows
    • Assisting in CAPA management/tracking
 
Qualifications:
  • Bachelor’s Degree required, PMP certification preferred
  • At least 5 years of relevant industry and drug development experience and exposure to Clinical Data Management preferred
  • Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors
  • Sound knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management
  • Strong comprehensive project management skills including expertise in metrics analysis and reporting methodologies
  • Strong oral and written communication skills with the ability to communicate effectively with senior management and cross-functional teams
  • Strong organizational skills and problem solving skills with a track record of delivering on time with quality
  • Significant experience with Microsoft Excel, PowerPoint and Project
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Paul Quibuyen
Christian.Quibuyen@eclaro.com
6466952942
Paul Quibuyen | LinkedIn
 
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.

Application Instructions

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