Remote Senior ICF Medical Writing Project Manager

ThermoFisher Scientific; Chile; Remote; CLP 30,000,000 - 60,000,000; Full time

Job summary

Thermo Fisher Scientific in Chile is seeking a Senior ICF Medical Writing Project Manager to lead patient-centric medical writing projects focused on Informed Consent Forms (ICFs). You will manage timelines, budgets, resources, and ensure quality while liaising with clients and internal teams.

Responsibilities include developing project plans, tracking milestones, coordinating cross-functional teams, and mitigating risks to deliver compliant documents on schedule.

Qualifications

• Minimum 5 years of pharmaceutical/clinical project management experience.
• Experience in medical writing or clinical projects is required.
• Experience managing ICF content is advantageous.

Responsibilities

• Develop project timelines, budgets, forecasts, and contracts for assigned projects.
• Collaborate with cross-functional teams to meet project deliverables.
• Monitor timelines and resources; provide status updates and escalation as needed.
• Identify and mitigate risks to quality, budget, or schedule.
• Ensure compliance with quality processes across project documents.

Skills

Project management

Budgeting & forecasting

Stakeholder management

Regulatory knowledge

Written English proficiency

Education

Bachelor's degree in a scientific field

Job description

Thermo Fisher Scientific in Chile is seeking a Senior ICF Medical Writing Project Manager to lead patient-centric medical writing projects focused on Informed Consent Forms (ICFs). You will manage timelines, budgets, resources, and ensure quality while liaising with clients and internal teams.

Responsibilities include developing project plans, tracking milestones, coordinating cross-functional teams, and mitigating risks to deliver compliant documents on schedule.