Senior ICF Project Manager

🔥 0 minutes ago

🇲🇽 Mexico – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

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 with a primary focus on informed consent forms (ICFs) • Collaborate with internal and client teams • Manage project timelines, budgets, and resources • Ensure timely delivery and quality of projects and documents for internal and external clients • Build client relationships and identify and resolve client management issues • Develop, monitor, and adapt project plans, timelines, budgets, and forecasts • Develop project standards and contract modifications and liaise with other departments • Collaborate with cross-functional teams and lead team meetings • Prepare and monitor timelines and provide status updates • Review projects using tracking and management tools • Evaluate, escalate, or resolve risks to project quality, budget, or timeline • Ensure compliance with quality processes and requirements • Review and manage project performance metrics

🎯 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, including 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 skills with internal and external stakeholders • 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

• Global team environment • Collaboration and development opportunities • Scientific excellence-focused work environment