Fortrea

Fortrea

Sr. Clinical Project Manager or Clinical Project Manager II - Ophthalmology

Durham · Senior · Part-time

Sponsorship not specified$125k-$160kDetected 21 days ago
GCPProject ManagementForecastingExcelClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingPublic SpeakingMicrosoft Office

About the role

  • A successful Project Manager will bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery.
  • % of the above that requires overnight stay: up to 30%

Responsibilities

  • Partner with project team members and key stakeholders to oversee and manage project budgets, resources, and scope.
  • Develops and mentors team members in multiple areas of expertise and provides feedback as needed to respective line managers.
  • Lead the identification of project, financial and quality risk leveraging end to end risk management practices and quality by design principles.
  • Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem solving with the project and client teams.
  • Lead the adherence to project governance and issue escalation pathways, ensuring that project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
  • Project Managers will work to develop and lead high performing teams by collaborating with key stakeholders to manage all aspects of the end-to-end lifecycle of the project including scope, timelines, risk, and budget.
  • Demonstrated ability to lead by example and to encourage team members to seek solutions independently.

Requirements

  • Experience (Minimum Required):
  • Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
  • 5 years on clinical project management experience within a CRO or pharma
  • Experience in Project Management of the End-to-End Clinical Trial Lifecycle or
  • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
  • Experience managing projects in a matrix and virtual environment.
  • In collaboration with relevant departments, prepare and deliver presentations for new business as required.
  • University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Nice to have

  • Master's or other advanced degree.
  • PMP certification
  • Biotech experience
  • What do you get?
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Applications will be accepted on an ongoing basis.
  • Work Environment:

Compensation

  • Applications will be accepted on an ongoing basis.

Benefits

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • Paid time off (PTO) - Flex Plan

Equal opportunity

  • domestic and international travel
  • Learn more about our EEO & Accommodations request here.
Apply directly at Fortrea →Create a free account for alerts like thisView Fortrea immigration profile

This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.