Clinical Project Manager I, Ophthalmology

Clinical Project Manager I, Ophthalmology Fortrea is seeking an Ophthalmology Clinical Project Manager I to join our growing FSO team. The role requires 4+ years of global project coordination experience with mandatory ophthalmology experience. Candidates must be based in the United States. Job Overview 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, staying within budget, meeting the customer’s needs, and adhering to the contract. Project Manager I’s, under leadership direction, will collaborate with key stakeholders to manage the assigned aspects of the end‑to‑end lifecycle of the project, including scope, timelines, risk, and budget. Responsibilities 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 adhere to professional standards and SOPs. Take accountability for driving project performance while meeting customer needs and maintaining operational excellence, including 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 address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements. Foster a positive client experience by serving as the 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. Assist project team members and key stakeholders to effectively manage budget, resources, and scope, and forecast project revenue, manage project costs, track resource needs, and contribute to contingency planning. 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. Perform all other duties as needed or assigned. Qualifications (Minimum Required) University/college degree (life science preferred) or certification in a related allied health profession (e.g., nursing, medical or laboratory technology) from an accredited institution. Five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) Minimum of four (4) years of relevant clinical research experience in a pharmaceutical company/CRO. Greater than four (4) years supervisory experience in a health care setting, with at least two (2) years of clinical research experience (including monitoring) in the pharmaceutical or CRO industries. 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 diseases. Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, PowerPoint). 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 prioritize workload for self and team. Demonstrated organizational skills and 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. Preferred Qualifications Local project coordination and/or project management experience. Proven experience managing global clinical trials across multiple regions with an understanding of cross‑functional and cross‑cultural considerations. Benefits Medical, Dental, Vision, Life, STD/LTD insurance. 401(K). Paid Time Off (PTO) – Flex Plan. Employee recognition awards. Multiple employee resource groups (ERG’s). Target pay range: $100–118K. Work Environment & Physical Requirements Work is performed in an office environment with exposure to electrical office equipment. Ability to sit for extended periods and operate a vehicle safely. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of fingers, hands, and wrists. Occasional crouching, stooping, frequent bending and twisting of upper body and neck. Ability to access and use a variety of computer software developed both in-house and off‑the‑shelf. Light to moderate lifting and carrying (or otherwise moving) objects including luggage and laptop computer with a maximum lift of 15–20 lbs. Regular and consistent attendance. Varied hours may be required. EEO Statement Fortrea is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. Individuals with accommodations may request assistance. Location Durham, United States. #J-18808-Ljbffr