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Medical Technical Writer, Fully Home Based - Ridgefield, United States - Maxis Clinical Sciences
Description
Job Description
Job DescriptionOutside EST ZONE candidate requested not to apply.
Duties:
Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams.
Manages all technical aspects of GMW document development as well as publishing and archiving activities and is the interface to Global Regulatory Operations.
Accountable for Patient Narrative process and final delivery including coordinating the strategy, overseeing the process, managing timelines with cross-functional teams, and interfacing and overseeing the vendor to ensure timely and successful document finalisation.
Responsible for the preparation of relevant content for global clinical documents (CTPs, IBs, CTRs, ICFs, or other relevant clinical documents) including the planning and set up in the document management system for authoring teams, the planning and strategy for document development, and the overseeing of timelines.
Requires proactive and continuous cross-functional coordination with functional areas outside of GMW as well as external vendors or CROs to ensure timely and successful document finalisation.
Manages and is accountable for all technical steps for document development.This may include the set-up, organization, and standard content management for various document types as well as overseeing and managing the publishing and archiving activities for global clinical documents managed by GMW.
The Medical Technical Writer serves as the interface between GMW and Global Regulatory Operations.
Ensures quality of the deliverables that are outsourced to vendors/CROs that are writing clinical trial reports or other clinical regulatory documents and acts as the interface with client's systems that are not accessible to external vendors.
Please only subimt candidate is EST and enter their location in the submisison. Candidates sitting in CST or PST will be rejected.
Skills:
The job involves working in global, cross-functional study and project teams, coordinating, and supervising a time-sensitive technical process with cross-functional involvement.
Sound knowledge of document management systems, clinical documents standards, clinical trials, their documentation, and regulatory requirements. Deep knowledge of international writing standards and conventions and regulatory writing. Sound knowledge of safety reporting and regulatory requirements. Ability to proactively identify problems and initiate improvements. Understanding of the business impact of timelines for clinical documents.
Excellent written and verbal English skills, sound knowledge of MS Office (especially Word, Adobe), Microsoft 365, document management systems, and high IT affinity.
Education:
Master's degree with a minimum of 2-3 years or a bachelor's degree with a minimum of 3-5 years of working experience, preferably in e.g. natural sciences, pharmacy, medicine or digital technologies, project management or communication science or any other relevant field with at least 3 years of professional experience preferably in clinical operations or related areas; alternatively vocational training, associate's degree, technical college e.g. in medical documentation or other relevant fields, with at least 5-8 years of professional experience and preferably 3 years of experience in technical writing, clinical operations or related areas.
Required Skills:
PROJECT MANAGEMENT
REGULATORY COMPLIANCE
ADOBE ACROBAT
DOCUMENT MANAGEMENT SYSTEMS
MICROSOFT OFFICE
Additional Skills:
EXCELLENT WRITTEN AND VERBAL COMMUNICATION SKILLS MEDICAL WRITING
Company DescriptionMaxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center.
The company provides 24×7 delivery globally, with teams across the world's 3 largest continents – North America, Europe and Asia.
We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication.It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.
Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.
Company Description
Maxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center.The company provides 24×7 delivery globally, with teams across the world's 3 largest continents – North America, Europe and Asia.
We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication.It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.
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Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.