14 Political Science jobs in Canada
Senior Consultant, Government Affairs (Alberta)
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Salary:
Position Overview:
Santis Health, a leading public affairs, communications and strategy consultancy focusing on the health care sector, has an opportunity for a Senior Consultant with our Government Affairs Practice. Based in Alberta and working remotely, this ambitious, self-motivated individual will work closely with the Santis government affairs team to provide strategic problem solving, public policy and government affairs to clients.
Applicants should have a sound knowledge of government affairs, public affairs, stakeholder relations and project management, as well as the most pressing health care and life sciences issues of the day. Previous experience working in health care, in the Alberta government or as a practicing consultant in Alberta would be an advantage.
Responsibilities Include:
- Working closely with Santis team members to manage a wide range of client projects and deliverables.
- Lead accounts and manage projects, ensuring ongoing client support, communication, development of project management plans, and fulfillment of overlapping deliverables.
- Advising on government engagement, public affairs, and advocacy strategies.
- Interacting with government officials and decision-makers to build and maintain relationships.
- Tracking emerging and evolving public policy issues and analyzing their implications to client organizations.
- Interact with clients and prospective clients, media, partner agencies, stakeholders and colleagues to build and maintain excellent relationships.
- Identifying key stakeholders and creating tailored stakeholder maps.
- Developing government relations initiatives, a wide range of briefing notes, slide decks and other products.
- Developing project management plans and keeping the project team focused on meeting multiple, tight timelines.
Qualifications:
- Degree in political science, public policy, economics, communications or a related field (or equivalent experience); post-graduate qualifications are beneficial.
- Minimum of 3 years of relevant work experience directly in the government or in a government relations role.
- Competencies in health care policy, networks in the health care sector and knowledge of the Alberta government and health care system is preferred.
- Demonstrated knowledge of government affairs, public policy and politics in Alberta, and across Canada.
- A solid mix of project management, policy analysis and communications experience.
Required Skills:
- Excellent written and oral communication skills.
- Strong research and analysis ability.
- Exceptional organizational skills with an ability to juggle multiple clients and projects.
- Skilled in priority-setting, efficient time-management and the ability to work independently.
- High level of professionalism.
- Flexible schedule for some evening/weekend work.
About Santis Health Inc:
Santis Health is a health care and life sciences consulting firm that provides a wide range of strategy, communications, and government affairs services to clients across Canada. Clients of Santis Health include some of Canadas largest companies from Pfizer, Medtronic and Roche to Shoppers Drug Mart and LifeLabs national health organizations like the Canadian Agency for Drugs and Technologies in Health (CADTH), the Canadian Partnership Against Cancer (CPAC) and the Canadian Institutes for Health Research (CIHR) and multiple hospitals, community organizations, and patient groups. To learn more, please visit:
Santis Health is dedicated to fostering a supportive and inclusive work environment that is safe and respectful. Our aim is to ensure all employees and job applicants are given equal and equitable opportunity, and that our organization represents a diverse array of expertise, skills and backgrounds. We are committed to fair employment practices that do not discriminate on the basis of age, gender, disability, socio-economic status, marriage and civil partnership, pregnancy and maternity, race, national origin, religious beliefs, political beliefs, sex and sexual orientation, and other dimensions that are intrinsic to who we are as individuals.
If you are interested in becoming the newest team member of Santis Health and believe you have the qualifications listed in the job description, please submit both your cover letter and resume here.
Project Officer, Governance, Regulatory & Government Affairs
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We are looking for the visionaries, the change-makers, the self-starters who are seeking more from their career. Change begins with the small decisions we make, each day, to support each other and strive to create inspiring incredible educational experiences for all students, no matter where they are or how they learn. This concept connects deeply to the idea that, in choosing a career with Yorkville University and Toronto Film School, you will have the opportunity to push boundaries, flex your creativity and inspire positive change for so many people. It’s also a call-back to the transformative power of education itself.
Our core values put the student experience at the center of what we do, reflecting who we are and aspire to be. If you want to shine a light on academic excellence, be empowered to make an impact on the transformation of the Canadian post-secondary education landscape, and work collaboratively beyond levels, join us.
Who we need
Reporting to the Senior Vice President, Governance, Regulatory & Government Affairs, we are looking for a Project Officer, Governance, Regulatory & Government Affairs, to join our team. Operating at the intersection of academic governance, government relations, regulatory compliance, and strategic communications, you will play a pivotal role in designing and operationalizing systems and tools that enhance institutional effectiveness, transparency, and alignment with Yorkville University's strategic goals. Through collaboration with both internal and external stakeholders, you will contribute to initiatives that enhance engagement, coordination, and visibility across a range of governance and compliance activities.
This is a full-time hybrid role, working 3 days per week in our downtown Toronto office.
What’s in it for you
Impact and ownership. You will have the opportunity to channel your curiosity and your drive, making measurable changes to the university through the project work you do. You will make a positive impact on the quality of the academic experience for thousands of students.
Influence and exposure. As a Project Officer, you will contribute to multiple projects, working cross-functionally to create and optimize how project teams communicate and organize plans through SharePoint, ensuring transparency and adherence to institutional policies. You will work closely with influential internal and external stakeholders, growing your visibility and network. You will build trusted relationships and become a go-to expert.
Career development. Yorkville University is a progressive, forward-thinking, innovative education centre. You will join an organization that inspires change, nurtures collaboration, supports faculty and students in their journey, and continuously innovates. You will work alongside a team that embraces every chance to learn, engage in professional development, and motivate each other, with opportunities to grow within the organization.
As our new Project Officer, Governance, Regulatory & Government Affairs, you will:
- Lead projects. You will support high-impact projects by applying sound judgment, attention to detail, and a collaborative, solutions-oriented mindset. You will lead the execution of cross-functional initiatives that advance academic governance, regulatory compliance, institutional research, and government relations priorities.
- Manage project administration. You will build and manage collaborative tools and infrastructure (e.g., SharePoint, Microsoft Teams, Smartsheet) to enable transparency, consistency, and effective project tracking for the team. You will maintain oversight of timelines and deliverables, ensuring clarity of roles, accountability, and progress across concurrent initiatives.
- Design and implement solutions. You will develop content such as briefing notes, internal communications, dashboards, and documentation that reflect institutional priorities and support decision-making. You will contribute to the development of frameworks and processes that enhance institutional readiness, data-informed planning, and responsiveness to stakeholder needs.
- Facilitate engagement. You will play a key role socializing projects, building consensus and gaining buy-in and engagement. You will organize consultations, track action items, and support governance and policy processes, ensuring the participation of internal and external stakeholders.
You have:
- The experience. You are driven by an insatiable motivation to build plans, solutions, and projects that come to life and work. Deeply curious, you continuously seek opportunities to learn and apply your knowledge to inform policies and create processes.
- The background. You have a Bachelor’s degree - it may be Public Administration, Education, Policy, Communications, or a related field- more importantly, you have the skills to take an idea and grow the concept, validating with research and analytics, and not just build but execute the plan. You may be familiar with academic governance, government relations, or survey data use.
- The interpersonal skills. You are an exceptional collaborator and communicator, able to build trust, gain buy in, influence without authority, and create genuine engagement. You have excellent written and verbal English skills. You can confidently work with internal and external stakeholders, including senior decision-makers and ministry representatives.
- The project management. You have experience coordinating cross-functional projects in a higher education or regulated environment. You are highly organized and detail-oriented, able to create and maintain project plans and manage project meetings and communications. You have strong time management skills and can balance multiple competing priorities while meeting deadlines. You are comfortable following structured processes and making decisions independently.
- The ownership. You are proactive, accountable, and driven to make a difference. You exercise sound judgment and can manage sensitive information with professionalism and discretion. You stay on top of what needs to be done, raise flags when necessary, and consistently deliver on time.
- The technical ability. You are proficient in Microsoft Office, Smartsheet, SharePoint and other collaboration tools. You can learn new systems quickly. You understand the importance of data accuracy, documentation, and audit readiness.
Why work at Yorkville University and Toronto Film School?
- An atmosphere that successfully blends an entrepreneurial culture with education. We value innovation and continuously look towards expanding our programming, working with the latest research, tools and solutions. As a private school with government approval of our offerings, we have the opportunity to do more, stay current and be future-forward.
- The chance to accelerate your career and disrupt education by responding to the needs you see and purposefully challenging the status quo. Everything we do here is about delighting and engaging our employees - and ultimately our students- from mentorship to teaching, from creative outlets to analytical ones.
- A place where all individuals feel welcomed in the academic and workplace environments and can bring their authentic selves to the educational and work spheres. We celebrate the full range of human diversity and we acknowledge that equal access to opportunities and services may require the removal of barriers that equity-seeking communities experience in trying to obtain this access.
- The opportunity to grow with access to free courses, certifications and programs - right up to our Masters' offerings.
Join us
We welcome and appreciate candidates with a range of backgrounds and experiences. If you have 70% of the qualifications we are looking for, express your interest.
What you can expect from our hiring process:
- A virtual interview with a Talent Advisor discussing your interest in the role.
- A virtual interview with the Senior Vice President, Governance, Regulatory & Government Affairs to discuss how your experience and approach align with the needs of the team and the organization.
- A case study exercise.
- A final in person interview with the Director of National Regulatory Affairs and the Director, Academic Governance, Policies, & Compliance followed by a further interview with the Senior Vice President, Governance, Regulatory & Government Affairs and a member of the leadership team.
Diversity, equity and inclusion are a critical component of life at Yorkville University and Toronto Film School and we are committed to making these values an integral part of our culture. We encourage applications from all qualified applicants, including women, persons with disabilities, Black, Indigenous and People of Colour (BIPOC), people from the Lesbian, Gay, Bisexual, Transgender, Transsexual, Queer, Questioning, Two-Spirit, Intersex, Asexual + (LGBTQ2SIA+) community and other equity-seeking groups.
Yorkville University is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act ('AODA'). If you require accommodation for disability, please notify Human Resources at 1- .
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Research Associate
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Reporting to the Ultimate Yield Research & Certification Manager, the Research Associate will play an integral role as part of the Ultimate Yield (UY) research team, contributing to agronomic research initiatives with the goal of optimizing crop production. This position will be responsible for establishing, maintaining and evaluating research plots with the intent of supporting data-driven insights to advance agricultural practices.
Position Responsibilities:
- Management of plots while maintaining strict adherence to research protocols
- Operation and basic maintenance of research equipment, including, but not limited to tractors, sprayers, plot drill, spreaders, combines, loading and securing equipment on trailers, driving trucks and trailers
- Planning and execution of field applications (i.e. seeding, spraying, harvesting etc.), including organization of inputs and materials needed
- Accurate and thorough in-field data collection
- Coordination with both research and agronomy teams to ensure all protocols are conducted at the correct time and stage (in-season field applications, data collection etc.)
- Regular scouting and maintenance of research plots
- Operation of technology used at research plots including drones, cameras etc.
- Problem solve issues observed in the field
- Assist the research team in sorting and organizing data
- Assist the Research Manager with planning of trials and protocols
- Contribute to team development of new trial ideas (field trials or technology to test)
- Assist Ultimate Yield advisors in-field activities as needed (soil sampling, scouting, tissue testing etc.)
- Other duties as required
EDUCATION AND EXPERIENCE:
- University Diploma or Degree with a focus on Agriculture
- Practical work experience in the agricultural sector
- Ideal candidate has farm equipment operating experience
OTHER REQUIREMENTS
- Exceptional time management skills and the flexibility to work longer and varied hours through peak season(s)
- Experience in crop scouting / crop diagnostics
- Excellent interpersonal skills and the ability to communicate effectively to all levels of staff and management
- Self-motivated and able to work independently with minimal direction
- Strong attention to detail with a focus on accuracy and confidentiality
- Mechanically inclined and able to troubleshoot and repair minor mechanical issues
Research Associate, Evaluation
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Company name: Blueprint
Position title: Research Associate, Evaluation
Physical location : Toronto, ON
Hybrid role – Available to work at least three days per week in office
Travel – Occasional travel within Canada
Employment status: Full-time, Regular
Hiring Range: $69,000 - $85,000
Vacancy status: Existing
About Blueprint
Blueprint helps decision-makers use data and evidence to tackle complex public policy challenges and improve outcomes for people across Canada. As trusted advisors to government, community, and industry leaders, we work across a wide range of policy areas, including employment, income security, mental health, child and youth development, housing, community safety, and justice.
Using an interdisciplinary approach, we deliver solutions that integrate policy analysis, strategic program review, applied research, data analytics, measurement, and evaluation—ensuring policies and programs maximize public value and make life better for Canadians.
About the role
As an Associate, you will play a central role in delivering high-impact work for our public sector and nonprofit clients. You will work as part of an inter-disciplinary team on projects that span evaluation, measurement, performance improvement, strategy, policy design, strategic program review, and service transformation. You’ll engage directly with clients, support evaluations, develop evidence-based insights, and contribute to practical solutions that inform decision-making and drive better outcomes.
You bring curiosity, strong analytical and reasoning skills and a familiarity with research methods. You are adaptable, organized, and able to manage multiple priorities while meeting deadlines efficiently. The ideal candidate thrives in a fast-paced environment, that blends rigorous evaluation and analysis with a collaborative, client-oriented approach. This is a great opportunity for someone who wants to work at the intersection of consulting, public policy and social impact—and who is excited by the challenge of using data and evidence to help governments solve complex problems.
Key responsibilities
- Work with clients to understand their challenges, define problems, identify goals and create evaluation frameworks and work plans
- Support primary data collection and analysis (e.g., programming and fielding surveys, cleaning and analyzing survey data, supporting interviews or focus groups, conducting thematic analysis of qualitative data, etc.)
- Facilitate client and stakeholder workshops, focus groups and interviews
- Contribute to project coordination and logistics including organizing meetings, taking minutes, updating workplans and tracking budgets
- Work collaboratively to interpret findings from multiple lines of inquiry and translate them into actionable insights, options and recommendations for our clients
- Draft high-quality client deliverables including briefing notes, presentation decks, reports, and knowledge mobilization materials
- Contribute to secondary research including literature reviews and jurisdictional scans
- Contribute to business development activities including project proposals and pitches
The successful candidate will demonstrate Blueprint’s values of being evidence-driven, people-centred, curious, accountable, and optimistic . They will contribute to communities of practice and professional networks both within and outside of Blueprint.
What we’re looking for
Minimum requirements
- Master’s degree in the Social Sciences (e.g., Economics, Urban Planning, Psychology, Public Health, Political Science), Public Policy, Global Affairs or Public Administration
- 2-5 years experience working in a public sector consulting and/or evaluation and research
- Experience with a range of applied research techniques and evaluation methodologies
- Policy domain knowledge in at least one of the following areas: employment, income security, mental health, child and youth development, housing, community safety, and justice
- Excellent oral and written communication skills, with a demonstrated ability to synthesize complex information into clear and concise client-facing materials
- High standards for accuracy, attention to detail and professional judgement
- A collaborative team player who brings curiosity, humility and an ability to work in a fast-paced, dynamic and agile work environment
- Strong time management and organizational skills; able to navigate tight timelines, actively communicate progress, proactively problem-solve
- Eagerness to contribute to a high-performance, feedback-oriented team culture
- Proficiency with Microsoft software (Word, PowerPoint, Excel) and willingness to learn and use other tools and platforms (e.g., Qualtrics, Miro, Condens)
To ensure team members are supported to do their best work, Blueprint provides:
- A mission-driven culture focused on public good and values learning and impact
- Growth opportunities and mentorship in a supportive environment
- Comprehensive medical, dental, and vision benefits, plus life and disability insurance and mental health supports through GreenShield+.
- RRSP matching of up to 6%.
- Monthly cell-phone allowance and a one-time stipend to support home-office set-up.
- Up to 18 days vacation annually, plus six universal leave days and year-end office closure (December 25 and January 1)
- Annual stipends for professional development, conferences, memberships and certifications.
We take care in ensuring that new team members align with our mission and are positioned for success in their roles. Please apply by September 12, 2025. Selected candidates will be invited to:
- Complete a short assignment that reflects the type of work an Associate would do
- Submit two writing samples
- Participate in an in-person interview at Blueprint’s Toronto office
Blueprint is strongly committed to equal opportunities in employment and reflecting the diverse communities we serve. We recognize that diversity enriches our approach to problem solving and contributes to an inclusive work environment. Thus, we welcome and encourage applications from people of all identities and lived experiences, including women, Indigenous Peoples, persons with disabilities, and members of the 2SLGBTQIA+ community. If your background or lived experience equips you for this role but doesn't exactly match the listed qualifications, please highlight this in your responses to the application questions.
Accommodations
Blueprint is committed to creating an accessible and inclusive workplace. We are committed to providing barrier-free and accessible employment practices in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). Accommodations are available on request for candidates taking part in the selection process. Please contact to ensure that we can best meet your needs.
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Research Associate, Preclinical
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Salary: $80,000-$100,000
Acuitas Therapeutics is a private biotechnology company based in Vancouver, British Columbia, Canada. We are the premier global provider of LNP delivery systems for nucleic acid therapeutics. Acuitas is partnered with multiple international, biotechnology and pharmaceutical partners who are focused on bringing new vaccines and drugs into clinical development and to the marketplace.
At Acuitas, we believe in combining excellent science with an enviable work culture. The advanced LNP technologies we provide for our partners are made possible by our employees who apply their passion, curiosity, and knowledge every step of the way. At Acuitas, you will have the opportunity to work as part of a close-knit team of exceptional scientists, who support the production of revolutionary technology that impacts the health and wellness of society. By living our values, including honesty, integrity, innovation and openness, we have fostered a supportive work environment where our employees feel empowered, challenged, recognized and rewarded. If you would like to work for a company that is at the top of the field, Acuitas is the company for you!
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other status protected by applicable law.
Job Title: Research Associate, Preclinical
YOU: A committed professional with experience in preclinical research looking to develop further in an innovative, fast paced biotech environment.
US: Leading innovators in the lipid nanoparticle (LNP) field, looking for a talented individual to join our collaborative, passionate, and diverse results focused team.
ROLE SUMMARY: Acuitas Therapeutics is seeking a Research Associate with a strong background in immunology and immunological methods to work in the Preclinical team, reporting to the Senior Research Scientist, Preclinical. The role holder will be responsible for executing and supporting studies assessing the pharmacology, immunology, mechanism of action, distribution and safety profile of our LNP, executing analyses and data interpretation, and presenting results to the team and company.
Working with the Preclinical team, the responsibilities would include:
- Executing and supporting studies to evaluate LNP activity, distribution, mechanisms of action, immune profiles and safety.
- Mastering established methods and developing new methods to support preclinical objectives, including ELISA, MSD, luciferase assays, qPCR, SDS-PAGE, DNA/RNA isolation and protein quantification.
- Cell culture and cell-based assays (including ELIspot), cell isolation, and processing tissues and fluids for downstream analysis.
- Hands-on experience in multi-colour flow cytometry, intracellular cytokine staining and gating strategies.
- General laboratory support including preparation of reagents and solutions, laboratory organization, maintaining sample and reagent inventory, and shipping of materials.
- Up to date Biosafety/Biosecurity (Containment Level 2+) and WHMIS certification will be required.
- Maintain familiarity with relevant scientific knowledge and advancements in LNP technology.
- May be required to train more junior staff and co-op students.
QUALIFICATIONS AND SKILLS:
- BSc with 2-10 years experience or an MSc with up to 7 years experience; some industry experience preferred.
- Hands-on experience conducting experiments with LNP in vitro and ex vivo; knowledge of LNP formulation processes, LNP characteristics, in vivo biodistribution, pharmacodynamics and pharmacokinetics
- Strong background in innate and adaptive immunology. Knowledge specific to LNP preferred.
- Strong understanding of cell biology and human physiology with a focus on liver structure and function as well as other fenestrated organs.
- Background in vaccine development and experience conducting/analyzing associated assays (ELISA, EliSpot, HAI)
- Hands-on experience in tissue isolation, single cell preparation, cell culture, cell-based assays and cell differentiation.
- Extensive experience in multiplex immune-based assays. Specifically Meso Scale Diagnostics and multichannel flow cytometry including the development of gating strategies.
- Confident and proven safety when working in Biosafety Level 2+ environments.
- Excellent writing and presentation skills. Accurate and appropriate data analysis and use of statistics.
- Familiar with Spotfire and Big Omics or similar visualization platforms. Fluent working with Graph Pad and Microsoft Office. Adept utilizing Flo Jo or similar.
- Responsible and reliable record keeping, organization and assisting in lab management as needed.
Lead Clinical Research Associate
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PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description- Coordinates investigator/ site feasibility and identification process, as well as study startup.
- Monitors project timelines and patient enrollment, implements respective corrective and preventive measures.
- Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region.
- Manages Monitors in the query resolution process, including Central Monitoring observations.
- Coordinates safety information flow and protocol/process deviation reporting.
- Performs clinical supplies management with vendors on a country and regional level.
- Ensures study-specific and corporate tracking systems are updated in a timely manner.
- Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager.
- Coordinates planning of supervised monitoring visits and conducts the visits.
- Manages the project team in site contracting and payments.
- Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager.
- Ensures ongoing evaluation of data integrity and compliance at a country/regional level.
- Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level.
- Oversees project team in CAPA development and implementation.
- Coordinates project team in process deviations review, management and reporting.
- Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs.
- Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead.
- Delivers trainings and presentations at Investigator Meetings.
- Prepares, conducts and reports site selection, initiation, routine monitoring and closeout visits.
- Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level.
- Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations.
- Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level.
- Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level.
- Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level.
- Ensures data integrity and compliance at a site level.
- Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer.
- Conducts project-specific training of site Investigators.
- Supports preparation of draft regulatory and ethics committee submission packages.
- Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience.
- Minimum of 5 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor.
- Must have prior experience monitoring or managing sites and CRAs in the United States with knowledge of US regulatory guidelines and practices.
- Experience with all types of monitoring visits in Phases I-III.
- Strong experience in Oncology preferred.
- Experience in CAR-T Therapy or other types of Cell Therapy, Gene Therapy, Radiation Therapy or Radiopharmaceuticals, or Nuclear Medicine is preferred.
- Strong experience in GI (Chron's, Ulcerative Colitis, IBS) preferred.
- Full working proficiency in English.
- Proficiency in MS Office applications.
- Ability to plan, multitask and work in a dynamic team environment.
- Excellent Communication, collaboration, and problem-solving skills.
- Ability to travel up to 65% (depending on project needs).
- Valid driver’s license (if applicable).
Additional Information
All your information will be kept confidential according to EEO guidelines.
For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
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