“eCRF” jobs in Canada

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• 2d

  Temporary Research Assistant I - Clinical Research Support Services, London Health Sciences Centre Research Institute

  Ontario

  Per diem

  LH

  London Health Sciences Centre

  2+ YOELondon Health Sciences Centre asks for a bachelor's degree in health sciences or a related field, or equivalent experience, plus at least two years of clinical research experience. Candidates need knowledge of clinical trial regulations, strong Microsoft Office and electronic data entry skills, and excellent English communication.

  Microsoft Office, eCRF, Lawson Research Management

• 3d

  Data Manager II

  Laval, QC +1

  RemoteFull Time

  

  Altasciences Company Inc

  Altasciences Company Inc needs a bachelor's degree in programming or a health science, or relevant experience instead. Candidates need clinical research understanding, strong communication skills, adaptability across data platforms and solid Microsoft Office skills.

  EDC system, eCRF, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, WebEx

• 8d

  Senior Clinical Data & EDC Programmer

  Burlington, ON

  On-siteFull Time

  IU

  ICR United States USA

  5+ YOEICON needs candidates with 5+ years of EDC programming in Medidata Rave and/or Veeva, plus SQL or SAS skills for vendor data and reconciliation work. R and Python are preferred, along with a bachelor's degree in a relevant field.

  Medidata Rave, Veeva, SAS, R, Python, SQL

  8d

  Principal Clinical Data & EDC Programmer

  Burlington, ON

  On-siteFull Time

  IU

  ICR United States USA

  10+ YOECandidates need 10+ years of EDC programming experience on Medidata Rave and/or Veeva, plus SQL and/or SAS skills. Experience leading studies and mentoring junior programmers, and a bachelor's degree in a relevant field, are required. R, Python and bid defense experience are preferred.

  Medidata Rave, Veeva, SAS, R, Python, SQL

• 10d

  Clinical Study and Regulatory Assistant

  Toronto, ON

  $28.18–$42.27/hrHybridFull Time

  UH

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

  Candidates need a community college diploma in a health-related field, at least 3 to 6 months of related experience, and high proficiency in Microsoft Excel. Knowledge of oncology, clinical trials and regulatory issues involving human subjects is required.

  Microsoft Excel, study databases

  14d

  Clinical Research Supervisor

  Toronto, ON

  $86k–$129k/yrHybridFull Time

  UH

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

  4+ YOE1+ MgmtCandidates need a health or science bachelor's degree, at least four years of oncology or clinical trial experience, and at least one year of leadership or mentoring experience. Strong organization, communication and computer skills are essential.

  REDCap, EDC systems, eCRF

• 10d

  Database Programmer

  Toronto, ON +1

  $75k–$125k/yrRemoteFull Time

  

  Alimentiv: Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.

  1+ YOEAlimentiv needs candidates with hands-on Medidata Rave EDC experience and independent C# programming skills. Candidates should have clinical database programming, eCRF and edit check experience, plus strong troubleshooting, communication and organizational skills.

  Medidata Rave EDC, C#

• 14d

  Associate Director, Clinical Data Management

  Canada

  Full Time

  M

  MSD

  15+ YOE15 years' clinical data management experience with an associate's degree, or 8 years with a bachelor's, or 4 years with an advanced degree; Deep experience with CDISC CDASH, SDTM and Controlled Terminology; Knowledge of

  Define.xml, CDISC tools

• 14d

  Associate Director, Clinical Data Management

  Canada

  Full Time

  

  Merck

  4+ YOEExpertise en normes de données cliniques CDISC (CDASH, SDTM, terminologie contrôlée); Connaissance approfondie des processus d'essais cliniques et des exigences réglementaires; Connaissance des directives ICH et BPC

  EDC, eCRF, CDISC standards tools, Define.xml

• 14d

  Associate Director, Clinical Data Management

  Canada

  Full Time

  

  Merck Sharp & Dohme LLC

  4+ YOEExpertise in clinical data standards development and implementation; Deep knowledge of CDISC CDASH, SDTM and Controlled Terminology; Experience in clinical trial data management and regulatory requirements

  Define.xml, SDRG, ADRG

• 26d

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

  Montréal, QC

  Remote

  

  Indero

  7+ YOECandidates 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

  26d

  Project Manager, Vendor Management / Gestionnaire de projet, gestion des fournisseurs

  Montréal, QC

  Remote

  

  Indero

  3+ YOECandidates need a B.Sc. in a related field, at least 3 years in clinical study management and 2 years coordinating clinical trials. Strong knowledge of GCP, ICH, FDA and Canadian regulations is required, along with excellent English communication; French is an asset.

  Microsoft Office, Trial Master File (TMF)

  26d

  Project Manager II, Early Phase (Canada)

  Montréal, QC

  Remote

  

  Indero

  5+ YOE3+ MgmtIndero 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)

  26d

  Project Manager II / Gestionnaire de projet II (Canada)

  Montréal, QC

  Remote

  

  Indero

  5+ YOE3+ MgmtBaccalauréat dans un domaine lié à la recherche clinique; Au moins 5 ans d'expérience dans l'industrie; Au moins 3 ans en gestion d'essais cliniques de phases I à III

  Microsoft Office, eCRF, TMF

  26d

  Project Manager / Gestionnaire de projet (Canada)

  Montréal, QC

  Remote

  

  Indero

  3+ YOEB.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

• 29d

  Clinical Safety Data Associate

  Markham, ON

  Full Time

  

  Everest New

  2+ YOEEverest Clinical Research needs candidates with an RN, MD, MSc, PhD or PharmD, or equivalent. They need two to three years of clinical trial data management experience, including medical coding and laboratory data, and strong written and oral communication.

  MedDRA, WHODrug

  29d

  Associate Director, Biostatistics

  Markham, ON

  Full Time

  

  Everest New

  10+ YOECandidates need a PhD in statistics or a related field with at least 10 years of relevant experience, or a Master's with at least 13 years. They must show exceptional performance and strong skills in statistical methods, regulatory requirements and team leadership.

  R

  29d

  Principal Biostatistician

  Markham, ON

  Full Time

  

  Everest New

  7+ YOECandidates need a PhD in statistics or a related field with at least 7 years of relevant experience, or a master's degree with at least 10 years and exceptional performance. Strong knowledge of clinical trial methodology, regulatory requirements and CDISC standards is essential.

  R

• 29d

  Concepteur de bases de données cliniques sénior, Sr. Clinical DB Designer

  Kirkland, QC

  Full Time

  I

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

  7+ YOEBaccalauréat en sciences, informatique, technologies de l'information ou technologie; 2 à 4 ans d'expérience pertinente en conception RAVE; 7 ans d'expérience totale minimum

  Medidata RAVE, InForm

11 companies