Remote Senior Technical Writer

New
  • Location
    Ottawa, Ontario
  • Job type
    Temporary/Contract
  • Category
    Science - Administration

Adecco is currently hiring for a Remote Senior Technical Writer for our Medical Manufacturer in Ottawa West. This is a full-time permanent position. Our client is offering full time hours Monday to Friday for this role. Compensation to be determined based on experience. Our client is offering remote work opportunity for this role.

To be considered for this Senior Technical Writer position you must have a minimum of 4 years experience in writing, editing and managing engineering and technical documentation utilized in the development of new products and improvement of existing products. As well as good working knowledge of personal computer software programs in Windows environment.

Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with-patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

Senior Technical Writer Overview:

This role is responsible for writing and editing clinical documents including study specific protocols and reports, and clinical procedures and SOPs. Constructs or secures the necessary analyses of metrics including quality system linkage and recommendations utilizing statistical methods and database tools available. Provide awareness of data anomalies and performance contrary to goal objectives to management.

Senior Technical Writer Responsibilities:

  • Writes or oversees writing of study-specific clinical protocols and reports. Responsible for gaining cross-functional alignment on content of documents.
  • Writes or oversees writing of clinical processes, procedures, SOPs, forms and other documentation as required.
  • Responsible for maintaining consistency across clinical documentation; writing and maintaining a glossary and style guide for use by other team members
  • Maintaining documents for clinical processes and procedures and ensuring compliance with GCP, regulations and client corporate policies.
  • Manages document update process; responsible for portfolio of clinical procedural documents and ensuring that current revisions are accurate and unambiguous.
  • Identifies, leads and implements process improvements in the management and writing of clinical documents.
  • Supports and helps draft publications arising from clinical studies.
  • Liaison with QA in the management and writing of clinical QRs in the CAPA process.
  • The output provided by this role is subject to external audit (e.g. FDA,ISO). The lack of accuracy and timeliness will impact the Quality system at site and division levels.
  • Ensure close communication and working relationship with R&D, regulatory, quality, PMO and other necessary functional teams
  • Provide supervision and mentorship to staff for their development and performance reviews
  • Provide updates to Senior management team as required
  • Senior Technical Writer Required Education and Experience:

  • A University degree is preferred (Science, Medical Technology or equivalent technical degree) or equivalent experience.
  • Three to six years of related work experience is required.
  • Strong verbal communication and interpersonal skills
  • Relevant experience Clinical Research or in a related area such as Technical Product Development, Quality or Regulatory in a healthcare industry.
  • Relevant experience Clinical Research or in a related area such as Technical Product Development, Quality or Regulatory in a healthcare industry.
  • IVD experience is preferred.
  • To be considered for the Technical Writer contract, please click on Apply Now!

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    Reference number CA_EN_1_021956_1575350

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