United Kingdom onlyThe Role
As a QC Editor, you will be responsible for ensuring the accuracy and consistency of various documents and materials related to uMotif’s eCOA solutions.
Your primary focus will be on reviewing and proofreading study documentation, designs, screenshots, presentations, prototype questionnaires, investigator training brochures and sales material, to ensure adherence to source documentation, established standards and guidelines.
What will you do?
- Review and proofread a wide range of documents and materials to ensure accuracy, consistency, and adherence to requirements and company standards.
- Verify that content, formatting, grammar, punctuation, and spelling are correct and consistent throughout all documents.
- Proofread uMotif questionnaire design concepts against licenced source documents to ensure compliance with ISPOR Guidelines as well as confirming designs accurately reflect source materials.
- Collaborate closely with cross-functional teams, including professional services, technical operations, design team, sales and quality assurance, to address any discrepancies or issues identified during the QC process.
- Provide feedback and suggestions for improving document quality, clarity, and readability. Ensure internal consistency from numerous sources, define standards to be adopted by all.
- Maintain thorough documentation of QC activities and findings, including tracking and reporting of errors and corrections.
- Manage the QC request process, prioritising personal workload against a dynamic backlog of work
- Assist in the development and implementation of QC processes and procedures to enhance efficiency and effectiveness.
- Stay updated on industry trends, best practices, and regulatory requirements related to clinical trial documentation and QC.
What you need to succeed
- Prior experience working in the eClinical field, preferably in a QC or proofreading role.
- Excellent attention to detail and ability to maintain high levels of accuracy while working under tight deadlines.
- Strong understanding of clinical research terminology and documentation requirements.
- Proficiency in Microsoft Office Suite and familiarity with document management systems.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams.
- Ability to adapt to changing priorities and work effectively in a fast-paced, dynamic environment.
- Experience in the use of an EDMS (eg, Veeva Vault)
- Bachelor's degree in a relevant field, such as English, communications, or a related discipline.
uMotif is an equal opportunity employer
We positively encourage applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity.
We want everyone at uMotif to be comfortable bringing their true self to work.
That means acknowledging your personality, including the quirky bits, and bringing your interests, hopes, dreams, and even fears with you is fine, even if they don't seem relevant to your work.
