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  • Posted: Feb 17, 2025
    Deadline: Not specified
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  • Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $18 billion and approximately 55,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient ...
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    ICF Medical Writing Project Manager

    Job Description

    • At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
    • We have a vacancy for an ICF Medical Writing Project Manager based in a number of global locations.

    A day in the Life:

    • Develops project timelines, standards, budgets, and forecasts.
    • Collaborates with cross-functional teams to meet project deliverables.
    • Ensures timely achievement of final deliverables.
    • Advances or resolves risks to project quality, budget, or timeline.
    • Ensures compliance with quality processes and requirements.

    Keys to Success:

    • BS/BA (preferably in a scientific field) with a minimum of 2 years of relevant experience or an advanced degree with at least 1 year of relevant experience.

    Experience

    • Experience managing medical writing or clinical projects.
    • Experience in the pharmaceutical/CRO industry preferred.
    • Proven experience in medical writing (eg, Regulatory and/or plain language).

    Knowledge, Skills, Abilities

    • Proficient project management skills, including budgeting and forecasting.
    • Solid planning and organizational abilities.
    • Excellent interpersonal and communication skills; self-motivated.
    • Good knowledge of global regulatory and document development guidelines.
    • Effective decision-making and problem-solving skills.

    go to method of application »

    ICF Medical Writing Program Manager

    Job Description

    • At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

    Discover Impactful Work:

    • Lead patient-centric medical writing programs with a focus on Informed Consent Forms (ICFs). 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.

    Education

    • 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

    • Experience managing medical writing or clinical projects.
    • Experience working in the pharmaceutical/CRO industry.
    • Preferably, experience in medical writing (Regulatory and/or plain language).

    Knowledge, Skills, Abilities

    • Advanced skills in budgeting, forecasting, and resource management.
    • Expert planning and organizational skills.
    • Excellent interpersonal and communication skills.

    Method of Application

    Use the link(s) below to apply on company website.

     

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