
Senior ICF Project Manager
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in Mexico, +4 more countries.
• Oversee medical writing projects centered on patient needs, specifically focusing on Informed Consent Forms (ICFs).
• Partner with internal teams and clients for effective collaboration.
• Administer project timelines, budgets, resources, quality control, and deliverables for both internal and external clients.
• Cultivate client relationships while identifying and addressing client management concerns.
• Create, track, and modify project plans, timelines, budgets, and forecasts as necessary.
• Establish project standards, forecasts, and contract amendments; coordinate with other departments regarding modifications.
• Work alongside cross-functional team members and facilitate team meetings.
• Prepare and oversee timelines while providing status updates to escalation points.
• Review projects utilizing tracking and management tools.
• Assess, escalate, and mitigate risks that may impact project quality, budget, or timeline.
• Ensure adherence to quality processes and requirements.
• Analyze and manage performance metrics for assigned projects.
• A BS/BA in a scientific field is preferred, with a minimum of 5 years of relevant experience, or an advanced degree with at least 3 years of pertinent experience.
• Equivalent experience of over 5 years providing the necessary knowledge, skills, and abilities for the role.
• Proven experience in managing medical writing or clinical projects is essential.
• Experience in managing ICF content is a plus.
• Background in the Pharmaceutical/CRO industry is preferred.
• Medical writing experience, including regulatory and/or plain-language writing, is advantageous.
• Strong project management capabilities, including budgeting, forecasting, and resource allocation.
• Excellent planning and organizational skills.
• Strong interpersonal, problem-solving, judgment, and decision-making abilities.
• Proficient oral and written communication skills with both internal and external stakeholders.
• Effective negotiation skills.
• Familiarity with global, regional, national, and other regulatory and document development guidelines pertinent to patient-centric deliverables.
• A high degree of independence in decision-making and problem resolution.
• Fully remote work arrangement.
• Standard Monday–Friday work schedule.
• Opportunities for collaboration and professional development.
• Global team environment.
• Exposure to innovation and scientific excellence.
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