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Fortrea

Fortrea is a contract research organization (CRO) that provides advanced laboratory-focused services that help change lives. On a mission to deliver “life-cha

Project Manager I, Ophthalmology

Location

United States

Posted

16 days ago

Salary

$100K - $118K / year

Seniority

Senior

Bachelor Degree4 yrs expExperience acceptedEnglishGoogle Cloud Platform

Job Description

Project Manager I, Ophthalmology

Fortrea

• Project Managers own the operational strategy, determining the most cost effective and efficient means to successfully run and complete projects on time, while maintaining quality, remaining within budget, while meeting the customer’s needs and adhering to the contract. • Collaborate with key stakeholders to manage assigned aspects of the end-to-end lifecycle of the project. • Management of scope, timelines, risk, and budget. • Bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery. • Assist in the leadership of the core project team, as directed by team leadership to facilitate their ability to lead extended cross-functional project teams. • Assist in the successful design, implementation, tracking and maintenance of project plans for assigned projects. • Ensure that all staff allocated to assigned projects adheres to professional standards and SOPs. • Take accountability for driving project performance while meeting customer needs and maintaining operational excellence. • Maintenance of timelines and tracking project progress against contracted deliverables. • Proactively lead quality control and risk assurance activities to ensure project deliverables are met according to regulatory, internal, and client requirements. • Participate in the identification, tracking and maintenance of projects, financial and quality risks using appropriate data sources, dashboards, and risk management strategies. • Adhere 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. • Foster a positive client experience by serving as client primary contact for areas assigned by Project Leadership. • Engage in communication and collaboration with the client and project teams across a matrixed, multi-cultural environment. • Participate in the development of project strategy in collaboration with relevant departments. • Assist project team members and key stakeholders to effectively manage budget, resources, and scope. • Participate in forecasting project revenue and managing project costs in adherence to the budget. • Manage and track project resource needs and contribute to contingency planning for key resources. • Ensure that resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges. • Identify timely scope changes against contract to assist in the change order process. • Facilitate positive communication and teamwork. • Develop and mentor more junior team members and provide feedback as needed to respective line managers.

Job Requirements

  • 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
  • In lieu of the above requirement, candidates with five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered.
  • Minimum of four (4) years of relevant clinical research experience in a pharmaceutical company/CRO
  • In lieu of the above requirements, candidates with greater than four (4) years supervisory experience in a health care setting of which two (2) years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered.
  • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
  • Demonstrated experience managing or supporting ophthalmology clinical trials, with strong working knowledge of ocular indications, assessment methodologies, and retinal (posterior segment) disease.
  • Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
  • Ability to work with minimal supervision.
  • Excellent verbal and written communication skills.
  • Ability to set clear expectations for junior staff on projects.
  • Ability to resolve project-related problems and prioritizes workload for self and team.
  • Demonstrated organizational skills and the ability to prioritize multi-tasks.
  • Ability to understand and work with financial information.
  • Basic knowledge of project management processes.
  • Demonstrated ability to work within a matrix system.

Benefits

  • Medical
  • Dental
  • Vision
  • Life
  • STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) – Flex Plan
  • Employee recognition awards
  • Multiple ERG’s (employee resource groups)

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