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Document Production Specialist
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Document Production Specialist
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Document Production Specialist
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Document Production Specialist
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Document Controller
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Document Controller
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Leeds, United Kingdom Unite People Full timeUnite People are working with a construction specialist contractor to hire a Document Controller based in West Yorkshire. Working with a leading new-build, mixed use development contractor; you will be working as part of a vibrant, dedicated site team to manage their document control process on projects ranging from £10m - £100m in value. **Role...
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Document Controller
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Document Production Specialist
2 months ago
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Document Production Specialist
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Document Production Specialist
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Clinical Document Specialist
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Document Administrator
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Document Administrator
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Clinical Document Specialist I
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Document Production Operator
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Document Production Operator
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Paralegal - Japanese Speaking - Document Review
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Estate Document Controller Officer
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Business Support Specialist
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Document Specialist
2 months ago
Document Specialist I, UK, remote
As one of the largest Clinical Research Organizations in the world, operating four ultramodern Clinical Research Units globally, the jewel in the crown is our facility in the UK (Leeds.) A brand new, world class, state-of-the-art 65,000 ft² clinic with 100 beds (and growing), fully dedicated to Phase I Clinical research.
This is a remote/ home-based, full-time, and permanent position in the UK.
Are you looking for a fresh start within a clinical document environment? Interested in working within Clinical Pharmacology, working alongside our Project Management and Phase I Monitoring team, in an administrative and IT-focused opportunity?
Fortrea is seeking a Clinical Document Specialist to join the global Clinical Pharmacology Services team. Perhaps you have some experience within a medical/life sciences environment but now looking to be home-based, managing documentation compliance across the clinical trial process.
Key Responsibilities
Responsible for general maintenance and any required archival of documents produced by the study project teams within CPS.Organizing, gathering, scanning, and filing of all applicable documents into appropriate electronic and/or paper copy locations, including the Trial Master File (TMF), as directed by Fortrea SOPs or other applicable directive.Responsible for document query generation and file reconciliation/resolution activities to support delivery of the TMF to client quality and integrity specifications, as well as to meet project timelines and productivity targets.Maintains an internal standardized filing structure for study-related documents.Works directly with the assigned Study Project Manager (PM) to review and finalise the TMF Plan and Index for individual projects.Creates and/or maintains any general document/file-related tracking forms and/or spreadsheets, as applicable.Maintains the TMF by working with applicable project team members to retrieve, file, and upload documents in accordance with applicable SOPs, policies, system, and client requirements.May interact directly with project teams in securing documents for the TMF, as appropriate.May interact directly with project teams to follow up regarding missing documents, as appropriate.Performs archiving duties for all paper and/or electronic media, as needed.Maintains departmental files including, but not limited to, project files.
Experience
Any experience within an administrative or IT-focused role within clinical trials or a hospital/medical setting would be advantageous. Full training will be provided.Experience working with computers and basic programs (i.e., Adobe Acrobat, Word, Excel, PowerPoint).
Education / Qualifications
High School Diploma or equivalent.Strong written and verbal communication skills (English language).Strong organisational skills, with the ability to work in a fast-paced setting with many interruptions.
Embark on a fulfilling career as you support us on our mission “To help make life-changing healthcare solutions possible”. Apply now and be part of an extraordinary journey.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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