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Certara: 1985- Sr. Analyst/Consultant, Epidemiology/Pharmaco-Epidemiology

Certara

This is a Full-time position in Montreal, QC posted July 26, 2021.

At Certara, we accelerate medicines to patients by partnering with life science innovators.

Our Integrated And Proprietary End-to-end Platform With Biosimulation, Regulatory Science, And Market Access Solutions Combined With Our Strong Team Of Scientists And Subject Matter Experts Enable Our Clients To HaveIn the past 6 years, over 90% of companies that received new drug approvals by the FDA used our software or services.informed decision-making & reduced clinical trial burdenhigher R& D productivityimproved patient outcomes & increased patient access to medicinesaccelerated regulatory approvalCertara is a global team that fosters and nurtures a diverse and inclusive culture.

We are proud to be an Equal Opportunity Employer.

The collective sum of our individual differences, life experiences, knowledge, innovation, self-expression, and unique capabilities and talent represents a significant part of our culture, our reputation and our achievement.Together with our partners, we use biosimulation and technology-enabled services to transform drug discovery and development across all therapeutic areas and innovative therapies.

Sr.

Analyst /Consultant Epidemiology/Pharmaco-Epidemiology Job OverviewThis is a great opportunity for an early career Epidemiologist/Pharmaco-Epidemiologist/Public Health professional to join a team of highly skilled epidemiologists, statisticians, health economists and consultants.

The successful candidate will work closely with other senior scientific staff within the company.

This position will allow the Senior Analyst/ Epidemiologist to deepen his/her skills by writing protocols for observational studies using a variety of healthcare databases, primary and secondary data collection, as well as providing scientific and other technical input during conception, conduct and delivery of various research projects.Main Tasks & ResponsibilitiesDesign and drafts/Supports design and drafts of protocols for a broad range of pharmaco-epidemiological observational studies utilizing real-world databases, primary and secondary data collection, including but not limited to Health Clinical databases, National Health Registries, Disease databases, chart reviews, surveys etc.Conducts ad hoc literature reviews on real-world evidence, health economics and related matters.

Summarize and synthesize a wide range of medical and statistical information, including disease specific and pharmaceutical product researchProvides epidemiological input/research for CRF/eCRF development.

Follows the scientific aspects of projects, coordinates with the operational, data management and statistical teams, liaise with other consultants assigned to the project to ensure quality delivery of the projectParticipates actively/Supports in the development and conduct of the statistical analysis of studies with statisticians and modelers as required.

Participates in production of reports, presentations and publications.

Critically analyzes data (presents results and provides internal data analysis, both qualitative and quantitative) and provides strategic thinking with respect to interpretation of resultsParticipates in consulting in epidemiology and drug assessment.

Participates in bid defense.

Provides complex, secondary research from client issue to completionProduces complex analytics and communicate clearly via charts and graphsDeliver small projects independently and/or produce sub-components of projects of greater complexity, with oversight Interacts with clients, as required, with senior staff involvement, as needed.

Performs necessary administrative functions and additional tasks, as required Support senior personnel with activities required for business development from time to timeParticipate in company-sponsored training programs as required to ensure that skills are learned, maintained and focused accordingly Required Qualifications / ExperienceMinimum of Master’s Degree in Epidemiology, Public Health or other related field PhD in Epidemiology preferred At least 1 year relevant post-graduate work experience preferredRequired SkillsProfessional proficiency in English, written and spoken Experience designing/writing protocol for database or other observational studies Ability to work both independently and as part of the team Ability to effectively prioritize and manage multiple tasks and projects Other InformationThis position can be office based or work-from-home in the UK, EU, Canada or USA.Number of Employees Supervised: NonePercentage of Travel Required: 0% travelCertara is an Equal Opportunity Employer.

Certara does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law.

All employment is decided on the basis of qualifications, merit, and business need.