Emplois “Trial Master File (TMF)” au Canada

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• 13h

  Clinical Research Associate (Canada)

  Kirkland, QC

  Temps plein

  CC

  CAN Canada

  Baccalauréat scientifique ou en soins de santé préféré; Connaissance des BPC et des lignes directrices ICH; Maîtrise de Microsoft Word, Excel et PowerPoint

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, laptop, iPad, iPhone

  27j

  Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

  Kirkland, QC

  Temps plein

  CC

  CAN Canada

  3+ ansAu moins 3 ans d'expérience en surveillance sur site; Connaissance approfondie des BPC et de l'ICH; Baccalauréat scientifique ou en soins de santé privilégié

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, laptop computer, iPhone, iPad

  27j

  Associé(e) de recherche clinique (ARC) principal(e) or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2

  Kirkland, QC

  Temps plein

  CC

  CAN Canada

  2+ ansBaccalauréat scientifique ou en soins de santé exigé; Au moins 2 ans d'expérience en surveillance sur place; Connaissance des BPC et des lignes directrices du CIH

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPhone, iPad

  27j

  Associé(e) de recherche clinique (ARC) principal(e) or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2

  Kirkland, QC

  Temps plein

  CC

  CAN Canada

  2+ ansBaccalauréat scientifique ou en soins de santé exigé; Au moins 2 ans d'expérience en surveillance sur place; Connaissance des BPC et des lignes directrices du CIH

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPhone, iPad

  27j

  Associé(e) de recherche clinique (ARC) principal(e) or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2

  Kirkland, QC

  Temps plein

  CC

  CAN Canada

  2+ ansBaccalauréat en sciences ou soins de santé; Au moins 2 ans de surveillance sur place; Connaissance des BPC et des lignes directrices du CIH

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, laptop, iPhone, iPad

• 17h

  Senior Clinical Research Associate

  Télétravail au Canada

  TélétravailTemps plein

  PR

  Premier Research Group Canada Limited

  4+ ansCandidates need an undergraduate degree or equivalent health or science background, with 4+ years of clinical trial monitoring experience and knowledge of ICH/GCP and FDA, EU and ISO14155 regulations. Fluent English and host-country language, strong communication skills and a valid driver's licence are required.

  eTMF, web-based communication tools

• 5j

  Clinical Trials Associate

  Télétravail au Canada

  TélétravailTemps plein

  

  Jobgether

  1+ ansCandidates need a university degree or equivalent experience, at least one year in an administrative, clinical research or project support role, and strong organization. Excellent English communication, Microsoft Office skills and attention to detail are also required.

  Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Trial Master File (TMF), project portals

• 6j

  6-Month Contract - Trial Committee Manager - Remote/Hybrid (Independent Trial Committee Mgmt Experience Required)

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Syneos Health needs candidates with prior experience independently managing trial committees, adjudication and clinical trial documentation. Candidates should be able to mentor staff and communicate clearly with internal teams and customers.

  Electronic adjudication platform, Trial Master File (TMF)

  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 Research Associate - Canada

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, or equivalent experience. They need knowledge of GCP/ICH guidelines, good computer skills, strong communication skills and the ability to travel up to 75%.

  Electronic data capture systems, Trial Master File, Clinical data tracking systems

  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

  1 mois

  Clinical Research Associate - Sponsor Dedicated - Bilingual (French/English) Homebased- Quebec,Canada

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Candidates need fluency in both French and English, plus clinical monitoring experience and a working knowledge of ICH-GCP, relevant regulations and company SOPs. Strong judgment, adaptability to changing priorities and comfort with electronic data capture systems are expected.

  Electronic data capture systems, Tracking systems, Case report forms

• 15j

  Specialist/Associate, clinical trial

  Quebec

  Temps plein, Temporaire

  

  FOP Consultants

  1+ ansCandidates need a bachelor's or master's degree in science, 1 to 5 years of industry experience (preferably in pharmaceuticals), and clinical research experience. They should know ICH/GCP and Health Canada and FDA rules, have TMF/eTMF experience, and write well in French and English.

  eTMF, TMF, MS Office

• 20j

  Site Navigator I - Remote US & Canada

  Télétravail au Canada

  TélétravailTemps plein

  FF

  FTINC Fortrea Inc.

  2+ ansCandidates need a university or college degree (life sciences preferred) or 2-3 years of clinical research experience, with working knowledge of ICH/GCP and IRB/IEC rules. Fluency in English and the local official language is required.

  Trial Master File system, CRF systems

• 20j

  Site Navigator I - Remote US & Canada

  Toronto, ON

  Temps plein

  

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

  1+ ansCandidates need a life science or allied health background, or 2-3 years of clinical research experience with knowledge of ICH/GCP and IRB/IEC rules. They must be fluent in English and the local official language, and be able to manage several deadlines at once.

  Trial Master File systems, CRF systems, Computer software

• 27j

  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

  Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

  Mississauga, ON

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  3+ ansAu moins 3 ans d'expérience en surveillance sur site; Connaissance approfondie des BPC et de l'ICH; Baccalauréat en sciences ou santé privilégié

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, iPad, iPhone

• 1 mois

  Senior Project Manager / Chef de projet principal, Early Phase and Translational Research, Canada

  Montréal, QC

  Télétravail

  

  Indero

  7+ ansCandidates need a related B.Sc., at least 7 years of industry experience with 5 years in Phase I-III clinical trial project management and financial accountability, and experience leading multinational trials over $25M USD. Strong knowledge of GCP, ICH, FDA and Health Canada rules and fluent English are required; PMP and dermatology experience are assets.

  Microsoft Office, Trial Master File (TMF) system

  1 mois

  Project Manager II, Early Phase (Canada)

  Montréal, QC

  Télétravail

  

  Indero

  5+ ans3+ gestionIndero needs a candidate with a bachelor's degree in clinical research or a related field and at least 5 years in clinical research, including 3 years managing Phase I and II trials. Strong knowledge of GCP, ICH, FDA and Health Canada rules is required, with dermatology trial experience strongly preferred.

  Microsoft Office Suite, Trial Master File (TMF)

  1 mois

  Project Manager / Gestionnaire de projet (Canada)

  Montréal, QC

  Télétravail

  

  Indero

  3+ ansB.Sc. dans un domaine lié à la recherche clinique; Minimum 3 ans d'expérience dans l'industrie pharmaceutique, biotechnologique ou CRO; Au moins 2 ans de coordination d'essais cliniques

  Microsoft Office, Excel

• 1 mois

  Clinical Research Associate

  Ottawa, ON

  80k–85k $/anContrat, Temporaire

  

  adecco

  2+ ansCandidates need at least 2 years of experience conducting clinical studies and knowledge of clinical research regulations and quality standards. A science bachelor's degree is preferred, and experience with medical devices, diagnostics or Veeva TMF is an asset. Candidates must be legally eligible to work and reside in Canada.

  Veeva

• 1 mois

  Clinical Research Associate

  Mississauga, ON

  60k–75k $/anHybrideTemps plein

  

  Profound Medical: (NASDAQ:PROF) is a commercial-stage medical technology company based in Mississauga, Ontario, advancing the standard of care for prostate cancer and…

  1+ ansCandidates need a bachelor's degree in biomedical sciences, ideally an MSc or research experience, and 1-3 years of clinical trial experience. They must know GCP, ethics and regulatory requirements, and communicate clearly while travelling up to 60% of the time.

  Clinical research, Analyse issues, Monitor activities, Documentation, Inspection, Improve business processes

• 1 mois

  CRA - Future roles (Canada)

  Toronto, ON

  HybrideTemps plein

  SH

  Syneos Health Canada LP

  Candidates need a bachelor's degree or RN in a related field, knowledge of Good Clinical Practice and ICH guidelines, good computer skills, strong communication skills, and the ability to travel up to 75% of the time.

  Electronic data capture systems, Tracking systems

13 entreprises