Senior Clinical Writer Jobs

Adecco is currently hiring a temporary full-time Senior Technical Writer to work for our client, a leading research and manufacturer of healthcare devices, in Ottawa, ON. In this role, you will be responsible for writing and editing clinical documents including study-specific protocols and reports, clinical procedures, SOPs, and CAPA documents. This role requires a bachelor’s degree in Science, Medical Technology, or equivalent technical degree or equivalent combination of education and work experience as well as 3 or more years of relevant experience such as Clinical Research or in a related area.

• Shifts: Monday to Friday | 8:00 AM – 5:00 PM
• Location: Ottawa, ON
• Job type: Temporary | Full-time

Here's why you should apply:

• The new and quicker onboarding process
• Paid weekly accurately and on time
• 4% vacation paid weekly
• Free training programs
• Strong health and safety programs
• Medical and dental benefits once qualified

Responsibilities:

• Ensures close communication and working relationships with R&D, regulatory, quality, program management, and other functional teams in order to achieve documentation deliverables. Maintains awareness of overall project timelines.
• Identifies process improvements in the management and writing of clinical documents.
• Responsible for maintaining consistency across clinical documentation; writing and maintaining a glossary, style guide, and templates, as appropriate, for use by other team members.
• Verifies and assesses the accuracy, consistency, and completeness of data and information in reports and documentation. Able to identify and access the sources of information needed to resolve issues.
• Defines and/or conducts formal literature searches to support clinical or other business activities. Summarizes scientific publications clearly and concisely, as required.
• Writes of study-specific clinical protocols and reports. Responsible for engaging appropriate subject matter experts and gaining cross-functional alignment on the content of documents.
• Miscellaneous other duties may be required.
• May provide supervision and mentorship to junior staff.
• The output provided by this role is subject to external audit (e.g. FDA, ISO). The lack of accuracy, compliance, and timeliness will impact the Quality system at site and division levels.
• Writes or oversees the writing of clinical processes, procedures, SOPs, forms, CAPA documents, and other documentation as required.
• Maintains documents for clinical processes and procedures and ensures compliance with GCP, regulations, Quality System procedures, and Abbott corporate policies.
• Supports and helps draft scientific publications arising from clinical studies, as required.

Qualifications:

• Writing, editing, and managing technical documentation utilized for clinical research, IVD or medical device regulatory submissions Quality System documentation, or the development of new medical products.
• Excellent written and oral communication skills with the ability to produce top-quality, error-free, and grammatically correct written work.
• Bachelor’s Degree in Science, Medical Technology, or equivalent technical degree or equivalent combination of education and work experience
• IVD Experience Preferred
• Experience writing CAPA documents is desirable. Knowledge of division products and Quality systems, system linkages, and quality measures is desirable.
• Minimum of 3 years of relevant experience in Clinical Research or in a related area such as Technical Product Development, Quality, or Regulatory in a healthcare industry.
• In-depth knowledge of software programs including Word and Adobe Pro, in Windows environment.
• Must be legally eligible to work, and reside in Canada
• Ability to effectively work on multiple projects at the same time and to appropriately prioritize work.

Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.

Adecco is the largest staffing firm in Canada with over 40 locations and our passionate team is dedicated to finding you a job you’ll love. We offer one of the best benefits packages in the whole entire staffing industry and we like to have fun at work!

To find out more about Adecco Perks and what we can do for you please visit the link here: https://www.adecco.ca/en-ca/working-with-a-staffing-agency/adecco-perks/

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