Project Manager

  • Project management
  • Full time
  • 3 years ago

Job Information

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    No. of Openings 1 opening
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    Job Experience 4 years
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    Education Level Bachelor
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    Location Restrictions USA only

Job Description

Company Description

Clinical Ink is a global clinical trial technology company that is transforming the clinical trial experience. Founded in 2007, the Company’s proven and future-built eSource platform, which includes solutions for EDC replacement, eCOA, ePRO and more, accelerates time to value while delivering scientific results that matter. With offices in Winston-Salem, NC, and Philadelphia, PA, Clinical Ink is advancing the business model responsible for bringing new treatments to market.

Job Description

Clinical Ink is seeking an experienced, and energetic Project Manager to join our Project Management team! The Clinical Project Manager’s responsibilities will include:

  • Serves as primary point of contact for Clinical Ink customers, managing all aspects of the project life cycle, including project scope, budget, delivery, change controls, and reporting
  • Develops and manages detailed project plan, including timelines, communication plan, training plan, data transfer plan and implementation plan
  • Leads project kick-off meetings and facilitates the requirements gathering process with customers
  • Ensures all functional leads and project team members understand their role and project requirements
  • Coordinates internal project resources and third parties/vendors to ensure the flawless execution of projects
  • Monitors and tracks project progress and provides project status reporting
  • Ensures projects are delivered on-time, within scope and budget
  • Delivers Investigator Meeting presentations that demonstrate solid comprehension of protocol and use of SureSoure platform
  • Conducts training sessions, as required, with site staff and monitors/CRAs
  • Supports business development activities, including bid defense presentations, as required
  • Performs other activities, as required, to ensure overall project and company success


  • Bachelor’s degree or equivalent experience
  • 4 + years of relevant clinical trials experience within a Clinical Research Site, CRO or eClinical service provider in a project management role or other equivalent experience
  • Experience with eCOA/ePRO required
  • Experience working in data collection and management systems
  • Demonstrates excellent verbal/written communication skills
  • Experience working on global projects and managing cross-functional teams
  • Working knowledge of software delivery lifecycle and methodology
  • Working knowledge of GCP, ICH guidelines and relevant FDA regulations

Additional Information

Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.

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