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Project Manager II

Job Description

About the Opportunity

Clinical Ink is seeking a Project Manager II to join our Project Management team based remotely. The Project Manager II will be responsible for supporting their assigned projects and clients, managing all aspects of the project lifecycle, and interfacing with internal/external teams to execute flawlessly on project deliverables.

Responsibilities

  • Serves as primary point of contact for Clinical Ink customers
  • Manages all aspects of the project lifecycle, including project scope, budget, delivery, change control, and reporting
  • Responsible for overall management and oversight of large complex clinical studies and/or programs
  • 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
  • Coordinates internal project resources and third parties/vendors to ensure 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
  • Conducts training sessions with site staff and monitors/CRAs
  • Supports business development activities
  • Mentors other Project Managers or Associate Project managers
  • Performs other activities as required

About You

Qualifications:

  • 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
  • 2+ years project management experience required working on global projects and managing cross-functional teams
  • Proven experience of managing multiple projects concurrently
  • Experience working in data collection and management systems
  • Excellent verbal/written communication skills
  • Working knowledge of software delivery lifecycle and methodology
  • Working knowledge of GCP, ICH guidelines, and relevant FDA regulations

Eligibility

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.

Benefits

For benefits information, please visit the company website at www.clinicalink.com.

About Company

Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.