Emplois “CTMS” au Canada

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• 4h

  Senior Project & Business Process Analyst - Digital PMO

  Toronto, ON

  41,96–52,45 $/hHybrideContrat

  UH

  University Health Network: University Health Network (UHN) is Canada's largest research hospital, which includes Toronto General and Toronto Western Hospitals, Princess…

  3+ ansCandidates need an undergraduate degree, at least 3 years of project management, business analysis and data analysis experience, and experience with healthcare or clinical research projects. Strong project management standards, workflow mapping, management-level presentations and end-user training skills are required.

  MS Planner, Atlassian JIRA, ServiceNow, CTMS, eTMF, Epic

• 4j

  Research Coordinator

  Edmonton, AB

  Sur placeTemps plein

  

  University of Alberta

  Candidates need an undergraduate degree, or other education plus relevant clinical research experience, and at least six months coordinating trials with project management ability. They also need working knowledge of ICH GCP and NIH guidelines, a valid Alberta Class 5 licence and their own vehicle.

  Microsoft Word, Microsoft Excel, Google Docs, Google Sheets, CTMS, Online meeting platforms

• 7j

  Director of Finance/Controller - Clinical Research

  Toronto, ON

  TélétravailTemps plein

  

  ClinSurge Research

  7+ ans3+ gestionCandidates need a CPA designation, a Bachelor's degree in accounting or finance, and 7+ years of finance experience including 3+ years in a controller role. Strong knowledge of Canadian accounting standards, HST/GST and payroll, advanced Excel, and experience with accounting systems are required.

  Excel, QuickBooks, NetSuite, Sage, CTMS

  28j

  Clinical Research Site Manager - Toronto

  Toronto, ON

  Temps plein

  

  ClinSurge Research

  Candidates need experience in clinical research site operations, knowledge of GCP and SOP compliance, and people management skills. Strong problem-solving, communication and comfort with CTMS and quality systems are expected.

  CTMS, eISF

• 11j

  Sr. Clinical Research Associate

  Mississauga, ON

  86k–136k $/an

  

  Novo Nordisk

  5+ ansCandidates need a bachelor's degree in life sciences or a related field and 5+ years of CRA experience. They must know ICH-GCP, use clinical trial systems such as EDC, CTMS and eTMF, and be able to travel up to 70% of the time.

  EDC, CTMS, eTMF

• 13j

  Clinical Research Regulatory Compliance Lead

  Toronto, ON

  

  The Hospital for Sick Children (SickKids): The Hospital for Sick Children (SickKids) is recognized as one of the world’s foremost paediatric health-care institutions and is Canada’s leading…

  7+ ansCandidates need seven or more years of clinical trial experience, including managing regulated trials and knowledge of Health Canada, FDA, ICH-GCP, TCPS 2, GAMP 5, ALCOA+ and 21 CFR Part 11. A bachelor's degree in a health, life science, research or computer science field is required.

  EDC systems, eTMF/ISF systems, CTMS

• 13j

  Local Trial Manager, Sponsor Dedicated → Responsable local(e) des essais cliniques, dédié(e) au promoteur

  Kirkland, QC

  Temps plein

  I

  IQVIA: IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences…

  Expérience démontrée en gestion d'essais cliniques; Solide connaissance des lignes directrices ICH-GCP; Diplôme en sciences de la vie, santé ou domaine connexe, de préférence

  CTMS, eTMF, Microsoft Office

• 24j

  Senior Inside Sales Associate

  Mississauga, ON

  HybrideTemps plein

  

  Sitero LLC

  2+ ansCandidates need a bachelor's degree, 2 to 3 years of relevant sales experience, and previous experience with a CRO, pharma or biotech company. They need expert-level English, strong prospecting and CRM skills, and proficiency in Microsoft Office.

  Salesforce, Microsoft Word, Microsoft PowerPoint, Microsoft Excel

• 26j

  Clinical Trial Manager

  Toronto, ON

  Temps plein

  

  Fortrea: Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in…

  4+ ansCandidates need four or more years of clinical research experience, prior SSU and Clinical Trial Lead experience, and a degree or allied health certification. They must know GCP, ICH and regulatory guidelines and be fluent in English.

  Microsoft Office, EDC, CTMS, eTMF, Veeva Vault, Medidata

  26j

  Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal

  Montréal, QC +1

  Temps plein

  

  Fortrea: Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in…

  1+ ansFortrea needs candidates with one to two years of clinical research experience, bilingual French and English, and a university or college degree (life science preferred) or allied health certification. Strong organization, attention to detail, and comfort with CTMS and financial processes are required.

  CTMS, SUVODA, COMET, SAP

• 26j

  Bilingual Clinical Research Associate (CRA) – Clinical Research Coordinator Experience

  Canada

  

  Medpace, Inc.

  2+ ansCandidates need a life science bachelor's degree and at least 2 years as a Clinical Research Coordinator. They must be bilingual in English and French and know ICH E-6 and Health Canada clinical trial regulations.

  Microsoft Office, CTMS

• 26j

  Clinical Trial Assistant I

  Markham, ON

  Temps plein

  

  Everest New

  1+ ansCandidates need a bachelor's degree in life sciences or a related field, strong written and verbal communication, and expert Microsoft Office skills. Knowledge of ICH-GCP guidelines and experience managing electronic TMFs are required, and one year of administrative support experience is preferred.

  Microsoft Office, Trial Master File (TMF), Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), Interactive Web Response Systems (IWRS)

  1 mois

  Clinical Operations Lead I (Oncology)

  Télétravail au Canada

  TélétravailTemps plein

  

  Everest New

  7+ ansCandidates need a bachelor's degree or RN in a life science, seven years of clinical trial or monitoring experience, and thorough knowledge of ICH-GCP. Oncology experience is required, and strong leadership and a valid driver's licence are needed.

  CTMS, eTMF, Trial Master File

• 27j

  Senior Director Team Lead, Therapeutic Area Quality (GCP / Clinical Quality)

  Mississauga, ON

  TélétravailTemps plein

  GL

  GlaxoSmithKline LLC

  3+ ans3+ gestionCandidates need a science or quality-related bachelor's degree, demonstrated GCP and clinical quality expertise, pharmaceutical or clinical quality experience, and at least 3 years of management experience leading an international team. Experience with Veeva QMS and CTMS is also required.

  Veeva QMS, CTMS

• 27j

  Senior Director Team Lead, Therapeutic Area Quality (GCP / Clinical Quality)

  Mississauga, ON

  Temps plein

  

  GSK

  3+ ans3+ gestionCandidates need a scientific or quality-related bachelor's degree, demonstrated GCP and clinical trial quality expertise, and at least 3 years of supervisory experience leading a global team. Veeva QMS and CTMS experience and knowledge of oncology, immunology, respiratory and vaccines are also required.

  Veeva QMS, CTMS

• 29j

  Clinical Data Manager

  Ottawa, ON

  96k–110k $/anContrat

  

  Agilus Work Solutions: Experts in Specialized Talent for Nearly 50 years. Canada's largest, full service, privately-owned recruiting firm.

  6+ ansCandidates need a bachelor's degree in health, clinical or biological sciences and about 6 years of clinical data management experience. Experience with EDC, CTMS and FDA 21 CFR Part 11 compliant systems is required.

  EDC system, CTMS, Project management tools

• 1 mois

  Clinical Data Manager

  Ottawa, ON

  96k–110k $/anContrat, Temporaire

  

  adecco

  6+ ansCandidates need a bachelor's degree in a health or science field and at least 6 years in clinical data management, clinical research or trials. They should know EDC and CTMS systems, ICH-GCP and 21 CFR Part 11, and have strong communication and project skills.

  EDC systems, CTMS, CRF design tools

• 1 mois

  Clinical Data Manager - Point of Care (Ottawa)

  Ottawa, ON

  87k–128k $/anTemps plein

  

  Abbott Laboratories

  6+ ansAbbott Laboratories needs candidates with an undergraduate degree or equivalent experience and 6 to 10 years in clinical data management, electronic data capture and clinical trial management systems. Candidates should know GCP, FDA 21 CFR Part 11 compliance and a programming language such as SAS, R or Python.

  Zelta EDC, SharePoint, MS Office, SAS, R, Python

• 1 mois

  Registered Nurse

  London, ON

  Sur placeÀ la journée

  

  Centricity Research: The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical…

  Candidates need an active, unencumbered Ontario RN licence and skill in medication preparation, injections, phlebotomy and IV placement. Acute care or clinical research experience, especially Phase I to IV, is a plus, and active ACLS is preferred.

  CTMS

  1 mois

  Infirmière ou infirmier de recherche/Research Nurse

  Lévis, QC

  Sur placeÀ la journée

  

  Centricity Research: The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical…

  Membre en règle de l'OIIQ ou de l'OIIAQ avec permis valide; Compétences en prélèvements sanguins et préparation de médicaments; Expérience en soins aigus ou en recherche clinique

  CTMS, CRF

• 1 mois

  Senior Study Start-Up Specialist

  Télétravail au Canada

  TélétravailTemps plein

  BM

  BeOne Medicines (Canada) ULC

  3+ ansCandidates need at least 3 years of progressive clinical research or clinical operations experience, ideally in biotech, pharma, a CRO or a clinical site. They must know ICH/GCP, regulations and SOPs and be skilled in document negotiation and site relationships.

  CTMS, eTMF

• 1 mois

  Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)

  Québec, QC +1

  TélétravailTemps plein

  WC

  Worldwide Clinical Trials Holdings, Inc.

  5+ ansWorldwide Clinical Trials Holdings, Inc. needs candidates with 5+ years as a Clinical Research Associate, oncology experience, a 4-year degree or nursing degree, and fluent written and spoken English and French. Candidates must live in Canada.

  Microsoft Office, CTMS, EDC systems

• 1 mois

  Clinical Trial Manager II

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN, proven site management and monitoring expertise, and knowledge of GCP and ICH guidelines. Strong communication, conflict resolution and problem-solving skills and good computer skills are also needed.

  CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS

  1 mois

  Clinical Trial Manager - Full Service

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, proven leadership of teams and project milestones, and expertise in site management and monitoring. They also need knowledge of GCP/ICH guidelines, budget management, conflict resolution and good computer skills, and preferably experience with risk-based monitoring.

  CTMS, Electronic Data Capture (EDC), Trial Master File (TMF), eDiary, ePRO, IVRS/IWRS

19 entreprises