Responsibilities
- Possesses in-depth knowledge of the pharmaceutical sector, medical affairs operations, and criteria for health technology assessments.
- Has sufficient methodological expertise to supervise systematic literature reviews covering clinical, economic, or health-related quality of life outcomes.
- Identifies key factors affecting evidence integration and clearly conveys them in project documents such as feasibility assessments and analysis plans.
- Produces polished, client-ready materials including study protocols, statistical analysis plans, technical reports, and presentation slides.
- Engages in short-term resource planning discussions to support project needs.
- Coordinates with team members to manage delivery of project components while maintaining high-quality standards.
- Supports on-time execution and financial accountability for assigned projects or subcomponents.
- Estimates effort requirements, proactively identifies potential obstacles, and communicates adjustments and solutions to project leads when needed.
- Reviews study update materials such as slides and meeting minutes, serving as an independent scientific voice visible to the client.
- Takes the lead on client communications, including calls and emails, while involving senior experts when necessary.
- Develops growth plans and provides mentorship to direct reports.
- Assists in creating proposals and presentations under the guidance of senior team members.
- May attend new business meetings, including those focused on generating innovative research concepts.
Work Arrangement
Remote (Worldwide)
Team
Multi-level team structure with collaboration across sophisticated evidence synthesis projects.
Other
- Work 100% remotely from Canada or the US.
- Culture is similar to that of a start-up, but in a well-funded established global portfolio organization.
