Senior ICF Project Manager

🔥 1 hour ago

🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

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Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Lead patient-centric medical writing projects focused on Informed Consent Forms (ICFs) • Collaborate with internal, client, and cross-functional teams • Manage project timelines, budgets, forecasts, resources, and contract modifications • Serve as liaison with other departments on contract modifications • Lead team meetings and communicate project status • Prepare and monitor timelines to ensure contractual delivery of final deliverables • Review projects using tracking and management tools • Evaluate, escalate, and resolve risks affecting project quality, budget, or timelines • Ensure compliance with quality processes and requirements • Review and manage project performance metrics • Build client relationships and identify and resolve client management issues

🎯 Requirements

• BS/BA (scientific discipline preferred) with at least 5 years relevant experience or an advanced degree with at least 3 years relevant experience • Previous experience providing the knowledge, skills, and abilities to perform the job (comparable to 5+ years) • Experience managing medical writing or clinical projects required • Experience managing ICF content advantageous • Experience working in the pharmaceutical/CRO industry preferred • Experience in medical writing (e.g., regulatory and/or plain language) advantageous • Strong project management skills, including budgeting, forecasting, and resource management • Solid planning and organizational skills • Excellent interpersonal, problem-solving, judgment, and decision-making skills • Effective oral and written communication and strong negotiation skills • Knowledge of global, regional, national, and other regulatory and document development guidelines relevant to patient-centric deliverables • High degree of independence in decision-making and problem-solving

🏖️ Benefits

• Collaboration and development opportunities • Remote office environment

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