Medical Writer - Markham, Canada - Everest Clinical Research

Everest Clinical Research

Verified Company

Markham, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.

We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence.

Building on this foundation, Everest has successfully developed and established itself as a full-service CRO.

Everest's headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Little Falls (Greater New York City Area), New Jersey, USA, and Shanghai (Pudong Zhangjiang New District), China.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs.

A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength that's us that's Everest.

To drive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a
Medical Writer for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

Key Accountabilities:

Work closely with the Everest project team members assigned to the project to achieve project milestones according to the project timeline.
Checking the accuracy of the Table of Contents (TOC) compared to the headings within the report and ensuring proper alignment of TOC styles within the Table of Contents. Similarly, checking the accuracy of any List of Tables or List of Figures compared to the intext tables and figures.
Checking the accuracy and completeness of abbreviations within the List of Abbreviations compared to intext abbreviations used in the report and abbreviations used in the statistical tables, listings, and graphs (TLGs).
Verifying that protocolrelated information is accurately and consistently applied to the text of the report

Such protocol information includes:
study objectives, study design, primary and secondary endpoints, treatments and procedures, and adverse event reporting procedures.

Checking the accuracy of numbers within intext tables and report text against the source data (e.g., TLGs).
Verify the accuracy of references to the source tables and listings.
Ensuring that Word styles are consistently applied throughout the document.
Verifying the accuracy of quoted references in the report.
Checking the accuracy of a list of appendices in a report compared to the final appendices produced for the report.
Act as a lead medical writer in the preparation of clinical documents or scientific publications.

This includes, but is not limited to, the following:

With proper medical and study disease area experience, developing initial document shells or drafts using appropriate and approved templates and adhering to Everest or sponsor's writing styles and formats.
Providing appropriate and accurate interpretation of study results based on the provided background materials (e.g., study protocol, statistical analysis plan, Investigator's Brochure, literature references) and statistical analysis output.
Performing effective editing on assigned medical writing products to refine them, as much as possible and when time permits, before releasing them for internal and external review. Following the Everest governing documents to obtain review comments on the document drafts from internal (Everest team) and external (sponsor staff) reviewers.
Ensuring appropriate QC checks have been performed on the medical writing deliverables. Incorporating reviewers' comments/input into the draft documents and delivering the revised documents for additional review cycle(s). Following up on the QC findings until they are properly addressed. Finalizing documents for delivery to sponsors according to the established timelines.
Perform literature searches to support senior medical writers.
Perform document epublishing for CSRs and other clinical/regulatory documents to ensure that the final medical writing product meets specific document publishing requirements and timelines.

Document publishing activities include, but are not limited to the following:

Rendering the completed final Word report to PDF.
Acquiring all documents or appendices from the Sponsor and Everest personnel.
Creating hyperlinks and bookmarks and ensuring they have appropriate destinations and properties.
May perform a lead role in the timely completion of tables, listings and graphs (TLG) assembly packaging into Word