Role overview

In this role, the Consultant must work on multiple complex projects without compromising on quality. Drive, determination, and a self-disciplined approach to achieving results are necessary for successful performance. Proficiency at devising novel solutions to problems is important, as is the instinct to evaluate these ideas critically before communicating them. The Consultant will maintain ownership of, and accountability for, the projects they are on, make thoughtful, strategic recommendations based on their experience, ensure best practices and procedures are followed, and consistently communicate with clients and other team members. The Consultant must have exceptional attention to detail, strong communication skills, and the drive to consistently deliver high-quality work while adhering to project timelines.
Duties and Responsibilities
The duties of this job require a high degree of specialized expertise-based problem-solving skills and quick, but thoughtful, decision making. Specific tasks include:

Researching, writing, and referencing product-specific documents for the pharmaceutical industry—examples of documents include: clinical summaries, reimbursement submissions, value stories and dossiers, manuscripts, conference abstracts and posters/presentations, and health-economic model technical reports
Leading projects from start to finish, interacting confidently with clients, and providing strategic guidance when needed
Independently managing time to meet deadlines while being available for web-based meetings during working hours
Working within planned project timelines and budgets, and identifying out-of-scope requests in a timely manner
Implementing corporate business development strategies to win new work where feasible (e.g., recognizing client needs and advancing company products and/or services to meet those needs)
Accurately and consistently implementing editor, client, and management feedback
Working autonomously and collaborating remotely within a team environment
Occasional travel may be required

Qualifications/Requirements

Advanced or professional degree (MSc, PhD, PharmD, MD) in a scientific/medical discipline
Prior experience in either the pharmaceutical/CRO industry or at a medical communications agency
Demonstrated track record of success in a medical writing role in terms of years at a given employer, promotions, or value of deliverables responsible for
Exceptional written and spoken English
Expert user of MS Word, PowerPoint, Excel, and reference management software (such as EndNote)
Familiarity with common biomedical terminology
Confident and professional demeanour; comfort interacting with senior pharmaceutical company executives

Assets

Strong quantitative skills, with a deep understanding of how to report statistical analyses of clinical-trial and epidemiologic data
Familiarity with principles and terminology of cost-effectiveness and budget-impact analyses
Portfolio or examples to share that are not bound by confidentiality
Knowledge of AMA style, GPP3, and ICMJE guidelines

Compensation & Benefits

Expected starting salary of CAD $80,000
Annual compensation adjustments and bonuses that are fully transparent and performance-driven.
Comprehensive health coverage, including generous medical, dental, and vision plans to support your total well‑being.