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eCOA Project Manager

Fortrea

Canada

Remote

CAD 80,000 - 120,000

Full time

Today
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Job summary

Fortrea seeks an eCOA Project Manager to oversee the implementation and support of clinical eCOA systems. In this role, you'll lead project management tasks from study kickoff to system decommissioning, ensuring timely delivery and resolving technical issues. Join Fortrea to make a significant impact on clinical trials with opportunities for professional growth and competitive compensation.

Benefits

Opportunities for professional growth
Competitive compensation and benefits

Qualifications

  • 2-5 years in project management of eCOA and DCT systems.
  • Proficiency in translating business needs into system specifications.
  • Experience with clinical systems like CTMS, ePRO, IVRS.

Responsibilities

  • Oversee outsourced eCOA systems implemented within trials.
  • Manage process from RFP creation to User Acceptance Testing.
  • Review and approve project documentation, track timelines.

Skills

Project Management
Clinical Systems Knowledge
Problem Solving

Education

BA/BS or Associate degree

Job description

Join to apply for the eCOA Project Manager role at Fortrea

Remote based within Canada

Are you a passionate clinical research professional ready to lead groundbreaking trials? Join Fortrea as a eCOA Project Manager and drive clinical excellence!

About The Role

The eCOA Project Manager is responsible for the client’s study-specific eCOA system implementation, ongoing support, closeout, and decommissioning. Provides subject matter expertise, leads study-specific implementation, ensures on-time delivery, and resolves support issues.

Key Responsibilities
  • Oversee outsourced eCOA systems implemented within trials
  • Proactively follow up with Sponsor and Third-Party Vendors to ensure understanding of study and technology design, involving kick-off meetings with stakeholders
  • Manage the process from RFP creation to User Acceptance Testing (UAT) planning, execution, defect management, leading to System Go-Live
  • Post-production responsibilities include reviewing and approving documents (BRDs, configuration specs, project plans, UAT plans, manuals), tracking documentation, maintaining TMF, adhering to timelines, representing as eCOA SME, resolving technical issues, coordinating during maintenance, and assisting with data transfers and decommissioning
Qualifications
Minimum Requirements:
  • 2-5 years in project management of eCOA and DCT systems development and validation
  • BA/BS with 2 years experience or Associate degree with 5 years experience
  • Proficiency in translating business needs into system specifications
  • Experience with clinical systems like CTMS, ePRO, IVRS, Inform, etc., in pharma/biotech industry
Work Environment & Benefits
  • Opportunities for professional growth
  • Competitive compensation and benefits

Be a leader transforming clinical trials into lifesaving solutions. Apply today to join Fortrea and make a global impact!

Learn more about our EEO & Accommodations policy here.

Additional Details
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job function: Project Management and IT

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