
10.000+ Mitarbeiter
🏥 Gesundheitswesen
🧬 Biotechnologie
💊 Pharmazie
Healthcare • Biotechnology • Pharmaceuticals
Fortrea ist eine Organisation für klinische Forschung (CRO) mit über 30 Jahren Erfahrung, die sich der Beschleunigung der Entwicklung lebensverändernder Behandlungen widmet, indem sie umfassende klinische Lösungen für Biopharma- und MedTech-Unternehmen bereitstellt. Sie bieten eine Vielzahl von Dienstleistungen an, darunter das Management klinischer Studien, Dienstleistungen im Bereich Pharmakologie und regulatorische Strategien, die alle auf die Bedürfnisse ihrer Kunden zugeschnitten sind. Die Mission von Fortrea besteht darin, Patienten in den Mittelpunkt ihrer Arbeit zu stellen und durch maßgeschneiderte, datenbasierte Ansätze innovative Therapien schneller auf den Markt zu bringen.
🕒 vor 10 Tagen
🇺🇸 Vereinigte Staaten – Remote
💵 $140.000 - $185.000 / Jahr
⏰ Vollzeit
🟠 Senior
👷♀️ Projektmanager
👻 Geisterscore 0%
🗣️🇺🇸🇬🇧 Englisch erforderlich
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10.000+ Mitarbeiter
🏥 Gesundheitswesen
🧬 Biotechnologie
💊 Pharmazie
Healthcare • Biotechnology • Pharmaceuticals
Fortrea ist eine Organisation für klinische Forschung (CRO) mit über 30 Jahren Erfahrung, die sich der Beschleunigung der Entwicklung lebensverändernder Behandlungen widmet, indem sie umfassende klinische Lösungen für Biopharma- und MedTech-Unternehmen bereitstellt. Sie bieten eine Vielzahl von Dienstleistungen an, darunter das Management klinischer Studien, Dienstleistungen im Bereich Pharmakologie und regulatorische Strategien, die alle auf die Bedürfnisse ihrer Kunden zugeschnitten sind. Die Mission von Fortrea besteht darin, Patienten in den Mittelpunkt ihrer Arbeit zu stellen und durch maßgeschneiderte, datenbasierte Ansätze innovative Therapien schneller auf den Markt zu bringen.
• Oversee and manage domestic, regional, and/or global projects, sometimes under the direction of a Project Director • Develop and manage project teams, communications, risk, scope, schedule, cost, quality, and stakeholders • Ensure project variances are proactively mitigated and client expectations are met • Apply working knowledge of drug development and clinical trial execution • Compile and drive project documentation, ensuring accuracy and quality of regulatory data • Serve as key client contact and establish working relationships with client project teams • Lead core project teams and facilitate extended project teamwork across internal and external stakeholders • Serve as escalation point for project issues • Proactively identify and resolve conflicts • Understand project delivery strategy, costing assumptions, and budgets • Deliver projects to scope, schedule, cost, and quality requirements • Manage internal and external change control processes • Lead quality control and risk assurance activities • Create, manage, and revise project plans; monitor progress against plans • Ensure staff adhere to professional standards and SOPs; provide performance feedback • Develop and maintain project performance indicators and client-specified KPIs • Define project resource needs and establish succession plans • Prepare and deliver new-business presentations • Train and mentor PM Academy PCs • Potentially manage lines and develop talent • Align resources with current and forecasted work • Support onboarding, development, retention, and succession planning • Assess project management competencies and create development plans • Provide line management and technical support, including training, development, and performance reviews • Perform other duties as assigned
• Candidates must be based in the United States • 2-5+ years of global project management experience with experience in Oncology or Ophthalmology • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution • Fortrea may consider relevant and equivalent experience in lieu of educational requirements • Minimum of seven (7) years of relevant clinical research experience in a pharmaceutical company/CRO, including at least two (2) years of full project management responsibility • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs • Advanced computer skills, including Microsoft Word, Excel, Project, Access, and Power Point • Experience managing projects in a matrix and virtual environment • Excellent communication, planning, and organizational skills • Demonstrated ability to lead by example and encourage team members to seek solutions independently • Demonstrated ability to handle multiple competing priorities and utilize resources effectively • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system • Financial awareness and ability to actively utilize financial tracking systems • Good knowledge of project management processes • Ability to work independently and mentor junior project team members • Ability to negotiate and liaise with clients professionally • Ability to present to staff at all levels • Oncology or Ophthalmology experience • Master's or other advanced degree (preferred) • PMP certification (preferred) • Biotech experience (preferred) • Ability to sit for extended periods and operate a vehicle safely • Ability to access and use a variety of computer software • Regular and consistent attendance • Varied hours may be required
• 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) • Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits
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