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Clinical Writer Jobs

Clinical Scholar Jobs
By Royal Victoria Regional Health Centre At Barrie, Ontario, Canada
Previous experience with project implementation and/or change management experience and participation in process improvement initiatives an asset
Change management knowledge to include ability to coach and support staff with program initiatives
Specialty Certification with Canadian Nurses Association an asset
Formal training specific to education an asset
3 – 5 years current or recent clinical practice experience in acute care required
Recent (within the last 3 years) Critical Care and/or Emergency experience preferred
Protocol Writer - Clinical Trials
By Pharma Medica Research Inc. At Mississauga, Ontario, Canada
Must possess good computer skills and organizational skills. Experience with an electronic document control and management system would be a plus.
Ensure timely and accurate entries and updates into a computer management system required for clinical conduct.
3 or more years of pharmaceutical related experience in medical writing, preferably in a CRO.
Thorough knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines.
Strong knowledge of medical terminology, clinical trials, and clinical research.
Strong knowledge of processes with a desire to promote improvement. Ability to motivate and energize others with a positive, can-do attitude.
Clinical Consultant Jobs
By Ranch Ehrlo Society At Regina, Saskatchewan, Canada
Effective time management and organizational skills with the ability to prioritize.
Experience providing clinical leadership, guidance, support, and development to team members is an asset.
Strong leadership skills with the ability to inspire, motivate, mentor, and support others.
Strong assessment, counselling, and service (CARE) planning skills.
Exceptional interpersonal skills with the ability to form strong relationships and professional working alliances.
Knowledge of person-centred thinking and gentle teaching.
Senior Clinical Regulatory Medical Writer
By Parexel At Canada
Use your project management skills to lead teams to quality and timely deliverables
Use your clinical knowledge to write and edit clinical study documents
Excellent interpersonal, verbal, and written communication skills.
Competent working in a matrix environment and values the importance of teamwork. Possesses team leadership skills and cross-cultural sensitivity.
Extensive clinical/scientific writing experience is required and consists of multiple clinical documents: study reports, study protocols, CTD documents and/or similar.
Lead Medical Writing experience with late phase documents (protocols, CSRs, CTDs) (Phase III) is required.
Clinical Engineer - Clinical Engineering
By Nova Scotia Health Authority At Halifax, Nova Scotia, Canada
Knowledge and experience in applying federal regulations, laws and standards in a healthcare setting.
Proven experience in meeting planned objectives and ad-hoc requirements within a large and diverse biomedical equipment portfolio.
4 years experience in a health care setting
Clinical engineering certification would be considered an asset
Proven ability to manage projects with large capital budgets.
Proven tolerance for ambiguity, with experience working through unforeseen challenges and obstacles to achieve both immediate and ongoing goals.
Senior Proposal Writer (Clinical Services) - Remote
By Syneos Health At Canada
Strong project and process management skills with ability to lead and mentor others.
May perform other duties as assigned by line manager.
Expert knowledge of the drug development process including functional operations and regulatory guidelines and directives.
Advanced proficiency in Microsoft® Office Suite (Word, Excel, and PowerPoint). Experience with SharePoint and additional industry-related tools preferred.
Excellent oral and written communication skills; fluent in reading, writing, and speaking English.
Strong interpersonal, organizational, analytical and negotiation skills.
Clinical Designer Jobs
By BuzzClan At Toronto, Ontario, Canada

• Experience with Cerner Learning Framework and/or Wiki

Senior Clinical Writer Jobs
By Adecco At Ottawa, Ontario, Canada
Identifies process improvements in the management and writing of clinical documents.
Bachelor’s Degree in Science, Medical Technology, or equivalent technical degree or equivalent combination of education and work experience
Experience writing CAPA documents is desirable. Knowledge of division products and Quality systems, system linkages, and quality measures is desirable.
Medical and dental benefits once qualified
Excellent written and oral communication skills with the ability to produce top-quality, error-free, and grammatically correct written work.
In-depth knowledge of software programs including Word and Adobe Pro, in Windows environment.

Are you a talented Clinical Writer looking for a new challenge? We have an exciting opportunity for you to join our team and help us create compelling clinical documents that will make a real difference in the lives of our patients. If you have a passion for writing and a keen eye for detail, this could be the perfect job for you!

Overview Clinical Writers are responsible for creating and editing clinical documents such as protocols, clinical study reports, and investigator brochures. They must have a strong understanding of medical terminology and the ability to interpret and summarize complex clinical data. Clinical Writers must also be able to effectively communicate with other members of the clinical team. Detailed Job Description Clinical Writers are responsible for creating and editing clinical documents such as protocols, clinical study reports, and investigator brochures. They must have a strong understanding of medical terminology and the ability to interpret and summarize complex clinical data. Clinical Writers must also be able to effectively communicate with other members of the clinical team. They must be able to work independently and as part of a team. Job Skills Required
• Excellent written and verbal communication skills
• Strong understanding of medical terminology
• Ability to interpret and summarize complex clinical data
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office
• Knowledge of regulatory guidelines
Job Qualifications
• Bachelor’s degree in a related field
• At least 2 years of experience in clinical writing
• Knowledge of regulatory guidelines
Job Knowledge
• Knowledge of medical terminology
• Knowledge of regulatory guidelines
• Knowledge of clinical research processes
• Knowledge of clinical data analysis
Job Experience
• At least 2 years of experience in clinical writing
• Experience in creating and editing clinical documents
• Experience in summarizing and interpreting complex clinical data
Job Responsibilities
• Create and edit clinical documents such as protocols, clinical study reports, and investigator brochures
• Interpret and summarize complex clinical data
• Communicate effectively with other members of the clinical team
• Ensure accuracy and compliance with regulatory guidelines
• Monitor and review clinical data for accuracy and completeness