Clinical Quality Project Manager

Posted 3 Hours Ago
Be an Early Applicant
6 Locations
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Clinical Quality Project Manager leads document development, revisions, and approvals while ensuring project objectives and GCP standards are met.
Summary Generated by Built In
Clinical Quality Manager

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Quality Project Manager to join our diverse and dynamic team. As a Clinical Quality Project Manager at ICON, you will be responsible for leading and managing projects, ensuring successful execution and delivery of project objectives.

What You Will Be Doing:

  • Managing and drives all aspects of document development, revision, retirement, according to the team Charter, ensuring documents are written in alignment with procedures and quality standards.

  • Ensuring Document Owner is informed of the process to develop, revise, or retire a controlled document.

  • Supporting Document Owner with authoring. May author framework for new documents upon request and as appropriate.

  • Managing and drives collaborative review, ensuring relevant functional area representation and drives resolution of edits/comments in collaboration with relevant stakeholders.

  • Ensures completion of Learning Needs Assessment and Training Curriculum Impact Assessment.

  • Supporting Head of Procedural Excellence with Implementation planning in close collaboration with Document Owner and other relevant stakeholders.

  • Ensures final endorsement of document(s) prior to coordinating approval workflows in the Document Management System (DMS).

  • Facilitates document revisions and VeeDMS workflows with guidance and oversight from the Head of Procedural Excellence, CAPA Lead, and/or Goals Lead.

  • Performs non-GCO document reviews as delegated by Head of Procedural Excellence

Your Profile:

  • Very Strong English Language proficiency required (written and verbal)

  • Strong operational understanding of Clinical Trials and GCP

  • Very strong Project Management experience is a must - this person will be managing deliverables that depend on other people

  • Exemplary organization, communication, and meeting facilitation skills - this is critical. This person needs to be able to clearly articulate concepts both verbally and in writing and facilitate meetings efficiently.

  • Exemplary QC skills - this person needs to be detail oriented.

  • Life Sciences degree

#LI-Remote

#LI-RS1

    What ICON can offer you:

    Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

    Our benefits examples include:

    • Various annual leave entitlements

    • A range of health insurance offerings to suit you and your family’s needs.

    • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

    • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.

    • Life assurance

    • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

    Visit our careers site to read more about the benefits ICON offers.

    At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

    If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

    Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

    Are you a current ICON Employee? Please click here to apply

    Top Skills

    Document Management System (Dms)
    Veedms
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    The Company
    HQ: Dublin
    34,685 Employees
    Year Founded: 1990

    What We Do

    Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

    We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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