Talent.com

C%2B%2B developer Jobs in Toronto, ON

Create a job alert for this search

C%2B%2B developer • toronto on

Last updated: 7 days ago
  • Promoted
Clinical Scientist / Scientifique clinique, Canada

Clinical Scientist / Scientifique clinique, Canada

InderoToronto, ON, Canada
Full-time +1
The Clinical Scientist is responsible for medical writing activities at Indero.The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocol...Show moreLast updated: 7 days ago
  • Promoted
Controls and Automation Engineer

Controls and Automation Engineer

Signode CanadaNot Specified, Ontario (ON), Canada
Full-time
With over $2B in revenue, 80+ manufacturing facilities across 6 continents and over 9,000 employees worldwide, Signode is a leading manufacturer of a broad spectrum of transit packaging consumables...Show moreLast updated: 8 days ago
Application Developer

Application Developer

Randstad CanadaToronto, Ontario, CA
Temporary
Quick Apply
Full-Stack Developer (Front-End Focus) — In-Office 3-Month Contract Downtown Toronto.Our client is seeking a Full-Stack Developer with a strong front-end focus to join their downtown Toronto team...Show moreLast updated: 11 days ago
Developer

Developer

Info Resume EdgeToronto, Ontario, Canada
Full-time
Your main responsibilities will include : .Collaborating with crossfunctional teams including designers and backend developers to translate design concepts and user stories into interactive and respo...Show moreLast updated: 13 days ago
AEM Developer Senior AEM Developer

AEM Developer Senior AEM Developer

ValtechToronto, Ontario, Canada
Full-time
Our global workforce exists to unlock a better way to experience the world and that all starts with our workplace.The borderless framework we work in. As an AEM Developer you will play a decisive ro...Show moreLast updated: 30+ days ago
.NET Developer

.NET Developer

Astra North Infoteck Inc.Toronto, ON, ca
Full-time
Quick Apply
Designing, Developing, testing and maintaining software application using.Interacts with Key business & technology stakeholders to define, analyze and deliver requirements that reflect the need...Show moreLast updated: 27 days ago
  • Promoted
Automation Specialist - Ontario

Automation Specialist - Ontario

SignodeToronto, ON, Canada
Full-time
With over $2B in revenue, 80+ manufacturing facilities across 6 continents and over 9,000 employees worldwide, Signode is a leading manufacturer of a broad spectrum of transit packaging consumables...Show moreLast updated: 29 days ago
Director, Clinical Services, Laboratory Services, William Osler Health System

Director, Clinical Services, Laboratory Services, William Osler Health System

Odgers BerndtsonToronto
Full-time
Applications are invited for the position of.Director, Clinical Services, Laboratory Services.William Osler Health System (Osler), a hospital system which includes Brampton Civic Hospital, Etobicok...Show moreLast updated: 30+ days ago
Product Lead - Global Payroll

Product Lead - Global Payroll

RipplingToronto, Canada
Full-time
Rippling gives businesses one place to run HR, IT, and Finance.It brings together all of the workforce systems that are normally scattered across a company, like payroll, expenses, benefits, and co...Show moreLast updated: 30+ days ago
  • Promoted
Developer

Developer

AkkodisOntario, Canada, Canada
Full-time
Akkodis is currently searching for a.Crown Corporation client within the Ottawa, Toronto, Halifax, and Montreal area.Author technical specification documents and diagrams for client’s platforms and...Show moreLast updated: 18 days ago
Engineering Student Intern

Engineering Student Intern

Lincoln ElectricToronto, ON, CA
Full-time +1
Lincoln Electric is the world leader in the engineering, design, and manufacturing of advanced arc welding solutions, automated joining, assembly and cutting systems, plasma and oxy-fuel cutting eq...Show moreLast updated: 10 days ago
Software Engineer - Front End

Software Engineer - Front End

Veeva SystemsToronto, Ontario, Canada
Full-time
Veeva Systems is a missiondriven organization and pioneer in industry cloud helping life sciences companies bring therapies to patients faster. As one of the fastestgrowing SaaS companies in history...Show moreLast updated: 30+ days ago
Vice President, Mass Affluent

Vice President, Mass Affluent

Nicola WealthToronto, ON
Full-time
We have a lot to be proud of at Nicola Wealth.Our sophisticated financial planning, our diversified private investment funds and their exceptional performance, our 99% client retention rate and our...Show moreLast updated: 30+ days ago
Manager, Business Processes - Control and Compliance

Manager, Business Processes - Control and Compliance

BMOToronto, ON
Part-time
The Manager, Business Processes, Control and Compliance will be responsible to oversee Market Risk compliance program as a 2b function. As part of the Market Risk Governance team in the second line ...Show moreLast updated: 30+ days ago
Senior Software Engineer - TypeScript

Senior Software Engineer - TypeScript

Veeva Systems IncToronto, ON, United States
Full-time
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in hist...Show moreLast updated: 30+ days ago
Co-Founder / CTO (100 % remote) (m / f / d)

Co-Founder / CTO (100 % remote) (m / f / d)

EWOR GmbHToronto, Ontario, Canada
Remote
Full-time
We are looking to hire ambitious entrepreneurs to start and scale their own startups.We are serial entrepreneurs for example Paul Mller (founder Adjust 1. Petter Made (founder SumUp 8B) who are eage...Show moreLast updated: 16 days ago
Regional Property Manager - Residential

Regional Property Manager - Residential

HinesToronto, ON, CA
Full-time
When you join Hines, you will embark on a career journey fueled by vision and guided by leaders who set the standards of our industry. Our legacy is rooted in innovation and excellence, earning us a...Show moreLast updated: 30+ days ago
Director, Tlap Derivative Portfolio Manager

Director, Tlap Derivative Portfolio Manager

RBC - Royal BankToronto, ON
Full-time
The Director - Retail Liquidity Portfolio Management is a key member of the broader Corporate Treasury Markets' team.The incumbent will support the broader team manage ~$100Bn of CAD high quality l...Show moreLast updated: 30+ days ago
Clinical Scientist / Scientifique clinique, Canada

Clinical Scientist / Scientifique clinique, Canada

InderoToronto, ON, Canada
7 days ago
Job type
  • Full-time
  • Permanent
Job description

Job Description

Job Description

The Clinical Scientist is responsible for medical writing activities at Indero. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistical analysis plans, clinical study reports), as well as scientific publications.

This role will be perfect for you if :

  • You are a strong medical writer with demonstrated ability to produce high-quality scientific documents to support clinical research.
  • You enjoy learning continuously and keeping yourself informed.
  • Having an impact within a growing company with momentum motivates you.

RESPONSIBILITIES

  • Is accountable for own medical writing deliverables, including quality, stakeholder communication, resolution of project issues, and timeline management;
  • Collaborates to clinical development of Phase 1 / First-in-Man studies, Proof of Concept (POC) trials, Phase 2b – 3 studies, and Phase 4 / registry trials.
  • Contributes to study design and writes / reviews clinical study protocols / amendments ;
  • Reviews informed consent / assent forms, study reference manuals, statistical analysis plans, and mock shells of statistical tables / figures / listings ;
  • Reviews, analyzes, and interprets study data based upon scientific expertise and industry standard practices;
  • Writes / reviews narratives and clinical study reports;
  • Prepares scientific abstracts, posters, and manuscripts;
  • Performs on-line literature searches;
  • Provides documents with high quality in terms of scientific content, organization, clarity, accuracy, format and consistency;
  • May perform quality control review of documents prepared by other team members;
  • Participates in process improvement efforts of the department.
  • Our company : The work environment

    At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

    In this position, you will be eligible for the following perks :

  • Flexible work schedule
  • Full-time permanent position
  • Complete benefits ( RRSP, medical, dental, vision, vacation, personal days, virtual medical clinic, social activities)
  • Ongoing learning and development
  • Work location

    The successful candidate for this position is given the option to work from home anywhere in Canada, or from our headquarters in Montreal (in accordance with company policies and public health directives).

    Occasional visits to our Montreal headquarters may be required or encouraged.

    About Indero

    Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.

    Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

    Innovaderm only accepts applicants who can legally work in Canada.

    Description - Fr :

    Le Scientifique clinique est responsable des activités de rédaction médicale chez Indero. Cette personne rédigera ou contribuera à l'élaboration de documents cliniques et réglementaires (synopsis, protocoles d'études, plans d'analyses statistiques, rapports d'études cliniques), ainsi que de publications scientifiques.

    Ce poste sera parfait pour vous si :

  • Vous êtes un rédacteur médical expérimenté avec une habileté démontrée à produire des documents scientifiques de haute qualité pour supporter la recherche clinique.
  • Vous aimez apprendre continuellement et vous garder informé sur les nouveautés dans le domaine.
  • Avoir un impact au sein d’une compagnie en pleine croissance et en pleine lancée vous motive.
  • RESPONSABILITÉS

  • Est responsable de ses propres livrables de rédaction médicale, y compris la qualité, la communication avec les parties prenantes, la résolution des problèmes du projet et la gestion du calendrier;
  • Collabore au développement clinique des études de phase 1 / essais de première administration (FIM), des essais de preuve de concept (POC), des études de phase 2b - 3 et des essais de phase 4.
  • Contribue à la conception de l'étude et rédige et examine les protocoles et amendements des études cliniques;
  • Révise les formulaires de consentement éclairé et d'assentiment, les manuels de référence des études, les plans d'analyse statistique et les coquilles simulées des tableaux / figures / listes statistiques;
  • Révise, analyse et interprète les données d'étude en fonction de l'expertise scientifique et des pratiques standard de l'industrie;
  • Rédige et révise les rapports d'études cliniques;
  • Prépare des résumés, posters et manuscrits scientifiques;
  • Effectue des recherches de littérature en ligne;
  • Fournit des documents de haute qualité en termes de contenu scientifique, d'organisation, de clarté, d'exactitude, de format et de cohérence;
  • Peut effectuer un examen de contrôle de la qualité des documents préparés par d'autres membres de l'équipe;
  • Participe aux efforts d'amélioration des processus du département;
  • Profil recherché : PROFIL RECHERCHÉ

    Éducation

  • Maîtrise en sciences de la vie; un doctorat représente un atout.
  • Expérience

  • Expérience en rédaction de documents cliniques et réglementaires tels que les protocoles d'étude et les rapports d'études cliniques;
  • Expérience en en analyse et communication des données d'étude;
  • Aptitudes et connaissances

  • Bonne connaissance des bonnes pratiques cliniques et des règlements / lignes directrices applicables de Santé Canada et de la Food and Drug Administration (FDA).
  • Bonne connaissance du processus de développement des médicaments;
  • Excellentes compétences en rédaction anglaise; solides compétences en communication anglaise; le français est un atout;
  • Excellente maîtrise de Word;
  • Capacité à gérer des tâches variées et multiples, à organiser son propre travail et à prioriser la charge de travail;
  • Excellente attention aux détails;
  • Attitude axée sur le client;
  • Capacité à apprendre rapidement, bonne adaptabilité et polyvalent.
  • Notre entreprise :

    L’environnement de travail

    Chez Indero, vous travaillerez avec des collaborateurs compétents et dynamiques. Nos valeurs sont la collaboration, l’innovation, la fiabilité et la réactivité. Nous offrons un environnement de travail stimulant et des possibilités d’avancement intéressantes.

    Vous bénéficierez des conditions suivantes :

  • Flexibilité sur l’horaire
  • Poste permanent temps plein
  • Gamme d’avantages sociaux (REER, assurances médicales, dentaire, vision, vacances, journées personnelles, clinique médicale virtuelle, rabais sur le transport en commun, activités sociales)
  • Bureau à proximité du transport en commun (métro Saint-Laurent ou métro Sherbrooke)
  • Travail de la maison ou hybride; au choix
  • Formation et développement continus
  • À propos d'Indero

    Indero est une entreprise de recherche clinique contractuelle (CRO) spécialisée en dermatologie et rhumatologie. Depuis ses débuts en 2000, notre entreprise à taille humaine bénéficie d’une solide réputation autant pour la qualité de la recherche effectuée que pour la qualité des soins offerts, dépassant les attentes de ses clients. Basé à Montréal, Indero continue aujourd’hui sa croissance en Amérique du Nord et en Europe.

    Indero s’engage à assurer une approche équitable ainsi que des opportunités équivalentes pour tous les candidats. À ce titre, Indero fournira sur demande des accommodations aux candidats ayant un handicap, et ce, à travers toutes les étapes du processus de recrutement, si demandé.

    Indero accepte uniquement les candidats pouvant légalement travailler au Canada.

    Le genre masculin est utilisé sans discrimination et dans le seul but d'alléger le texte.

    Requirements : IDEAL PROFILE

    Education

  • MSc in life sciences; PhD is an asset;
  • Experience

  • Experience in writing clinical / regulatory documents such as study protocols and clinical study reports;
  • Experience analyzing and reporting on study data
  • Knowledge and skills

  • Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations / guidelines.
  • Good knowledge of drug development process;
  • Advanced English writing skills; strong English communication skills; French is an asset;
  • Strong proficiency of Word;
  • Ability to handle varied and multiple tasks, organize own work, and prioritize workload;
  • Has excellent attention to detail;
  • Client-focused attitude;
  • Quick learner, good adaptability, and versatile.