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Job Title:

ICF Medical Writing Program Manager

About the Role:

We are seeking an experienced ICF Medical Writing Program Manager to lead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs). The successful candidate will manage complex projects, engage with clients, and ensure flawless delivery and quality of documents, contributing to world-class research outcomes.

A Day in the Life:

• Develop and adapt project plans and timelines.
• Engage and manage client relationships.
• Collaborate with cross-functional teams.
• Monitor project progress and provide status updates.
• Mentor junior staff and ensure compliance with quality processes.

Keys to Success:

• Advanced project management skills.
• Outstanding planning and organizational abilities.
• Excellent communication, negotiation, and decision-making skills.
• In-depth knowledge of regulatory and document development guidelines.
• Proven ability to lead and mentor junior staff.

Requirements:

• BS/BA (preferably in a scientific field) with a minimum of 8 years of relevant experience, or an advanced degree with a minimum of 6 years of relevant experience.
• Experience managing medical writing or clinical projects.
• Experience working in the pharmaceutical/CRO industry.
• Preferably, experience in medical writing (Regulatory and/or plain language).

What We Offer:

We offer a competitive salary, an extensive benefits package based around the health and well-being of our employees, flexible working culture, and a collaborative environment where diverse experiences, backgrounds, and perspectives are valued.