Emplois “Clinical trial management system” au Canada

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• 2h

  Senior Manager, Regulatory Affairs

  Télétravail au Canada

  119k–187k $/anTélétravailTemps plein

  

  Jobgether

  5+ ansCandidates need a life sciences bachelor's degree, 5–8 years of regulatory affairs experience, and strong knowledge of Canadian regulatory requirements and Health Canada processes. Strong client leadership, communication and project management skills are also required.

  1j

  Principal Programmer - RWD/EPI

  Télétravail au Canada

  TélétravailTemps plein

  

  Jobgether

  5+ ansCandidates need a Master's or PhD in epidemiology, biostatistics or a related quantitative field, and at least five years of real-world evidence analytics experience. Strong SQL, SAS or R, and applied regression and survival analysis skills are required.

  SQL, SAS, R, Optum Clinformatics Datamart, Truveta, UK Biobank

  1j

  Patient Safety and Pharmacovigilance Specialist

  Télétravail au Canada

  TélétravailTemps plein

  

  Jobgether

  3+ ansCandidates need a bachelor's degree in a medical, nursing, pharmaceutical or life sciences field, with an advanced qualification strongly preferred. At least 3 years of drug safety or pharmacovigilance experience, working knowledge of Argus Safety, and familiarity with FDA regulations and ICH guidelines are required.

  Argus Safety, Microsoft Word, Microsoft Excel, Microsoft PowerPoint

• 7h

  Associate Clinical Data Manager- FSP, GI

  Toronto, ON

  TélétravailTemps plein

  FF

  FTCAN Fortrea Canada Inc.

  6+ ansCandidates need 6 to 8 years of clinical data management experience, including at least 1 year of direct sponsor management, plus a university or college degree (or equivalent experience) and fluent English. Knowledge of clinical trial processes, medical terminology and electronic data capture is needed, with EDC experience of 3+ years preferred.

  Electronic Data Capture (EDC) systems

  7h

  Senior Clinical Data Manager- FSP, GI

  Toronto, ON

  TélétravailTemps plein

  FF

  FTCAN Fortrea Canada Inc.

  8+ ans2+ gestionCandidates need at least 8 years of early or late-stage clinical data management experience, including 2 years managing sponsors and 2 years mentoring others. GI therapeutic area experience, a degree or equivalent experience, and English are required.

  EDC systems, SAS

• 7h

  Associate Clinical Data Manager- FSP, GI

  Toronto, ON

  Temps plein

  

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

  6+ ansCandidates need 6 to 8 years of clinical data management experience, including at least one year of direct sponsor management. A university or college degree or equivalent experience is also required, and English must be fluent.

  Electronic Data Capture systems, SAS

  7h

  Senior Clinical Data Manager- FSP, GI

  Toronto, ON

  Temps plein

  

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

  8+ ansFortrea needs candidates with at least 8 years of early or late-stage data management experience, including 2 years of direct sponsor management and 2 years of technical mentoring. A bachelor's degree or equivalent experience and GI therapeutic area experience are required.

  Electronic Data Capture (EDC) systems, SAS

• 8h

  CRA II

  Burlington, ON

  TélétravailTemps plein

  IC

  ICR Canada - CAN

  2+ ansCandidates need a life sciences, healthcare or clinical research qualification, or equivalent experience, plus at least 2 years as a CRA. They need in-depth knowledge of ICH GCP and site monitoring, and experience with site qualification, initiation, monitoring and closeout.

  CTMS, EDC, electronic trial master file

  1j

  Associate Clinical System Designer

  Burlington, ON

  HybrideTemps plein

  IC

  ICR Canada - CAN

  1+ ansCandidates need at least 6 months of experience designing clinical systems in clinical research, experience with clinical data management systems, and familiarity with Medidata Rave and/or Veeva EDC. A bachelor's degree in a relevant field and excellent written and verbal communication are also required.

  Medidata Rave, Veeva EDC, clinical data management systems

• 9h

  Assistant(e) de recherche clinique 2/ Clinical Trials Assistant 2

  Mississauga, ON

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  3+ ansCandidates need a high school diploma or equivalent, 3 to 4 years of administrative support experience, and working knowledge of Microsoft Word, Excel and PowerPoint. Clinical research experience of at least one year is strongly preferred, along with basic knowledge of GCP and ICH guidelines and good written and spoken English.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint

  14h

  Assistant(e) de recherche clinique 2/ Clinical Trials Assistant 2

  Mississauga, ON

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  3+ ansCandidates need a high school diploma or equivalent, 3 to 4 years of administrative support experience, and working knowledge of Microsoft Word, Excel and PowerPoint. Clinical research experience of at least one year is strongly preferred, along with basic knowledge of GCP and ICH guidelines and good written and spoken English.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint

  14h

  Assistant(e) de recherche clinique 2/ Clinical Trials Assistant 2

  Mississauga, ON

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  3+ ansCandidates need a high school diploma or equivalent, 3 to 4 years of administrative support experience, and working knowledge of Microsoft Word, Excel and PowerPoint. Clinical research experience of at least one year is strongly preferred, along with basic knowledge of GCP and ICH guidelines and good written and spoken English.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint

  14h

  Assistant(e) de recherche clinique 2/ Clinical Trials Assistant 2

  Mississauga, ON

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  3+ ansCandidates need a high school diploma or equivalent, 3 to 4 years of administrative support experience, and working knowledge of Microsoft Word, Excel and PowerPoint. Clinical research experience of at least one year is strongly preferred, along with basic knowledge of GCP and ICH guidelines and good written and spoken English.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint

• 9h

  Experienced Clinical Research Associate (CRA II / Sr / PCRA) - Ontario Canada

  Alberta

  Temps plein

  

  Thermo Fisher Scientific

  1+ ansCandidates need a life sciences bachelor's degree or a nursing registration, plus about one year of clinical monitoring experience or the PPD Drug Development Fellowship. They must know ICH-GCP and clinical trial regulations, have strong critical thinking and communication skills, and hold a valid driver's licence where applicable.

  Clinical Trial Management System, Microsoft Office

• 9h

  Research Laboratory Manager - Institute for Mental Health Policy Research

  Toronto, ON

  94k–141k $/anSur place

  

  Centre for Addiction and Mental Health (CAMH): The Centre for Addiction and Mental Health (CAMH) is Canada's largest mental health and addiction teaching hospital.

  2+ ansCandidates need a bachelor's degree in a science or health discipline and at least 2 years in a research or laboratory setting with growing responsibility. Experience managing research staff or teams, knowledge of research ethics and regulations, and strong organizational and communication skills are required.

  Research, Mental health, Reporting, Presentation skills, Work independently, Leadership

• 11h

  Clinical Project Coordinator, IQVIA Biotech (home-based)

  Kirkland, QC

  Temps plein

  PI

  PY IQVIA RDS Inc.

  4+ ansCandidates need a bachelor's degree in life sciences or a related field and about 4 to 5 years of experience. They also need basic knowledge of GCP and ICH guidelines, strong English communication, attention to detail, and good MS Office skills.

  MS Office, IQVIA systems, Project tracking tools

• 11h

  Principal Medical Writer

  Ontario

  TélétravailTemps plein

  PI

  Parexel International (Canada) LTD

  Candidates need a Life Sciences or Health Sciences bachelor's degree or equivalent, extensive experience preparing clinical and regulatory documents, and experience managing complex projects. Advanced Microsoft Word skills and fluent written and spoken English are also required.

  Microsoft Word, SharePoint, Excel

• 11h

  Clinical Trials Associate - US/CANADA

  Ontario +2

  TélétravailTemps plein

  

  Worldwide Clinical Trials Co., Ltd.: The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support…

  1+ ansCandidates need a degree or equivalent professional experience, plus at least one year in a related role. Strong English, attention to detail, multitasking ability and proficiency in Microsoft Office are required, along with knowledge of ICH, GCP and FDA or EU regulations.

  Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Project portals

• 13h

  Experienced Clinical Research Associate (CRA II / Sr / PCRA) - Ontario Canada

  Télétravail au Canada

  TélétravailTemps plein

  PC

  PPD Canada, LTD.

  1+ ansCandidates need a life-sciences bachelor's degree or a Registered Nursing certification, plus about one year as a clinical research monitor or completion of the PPD Drug Development Fellowship. They need strong clinical monitoring, ICH-GCP, root cause analysis and communication skills, and a valid driver's licence where applicable.

  Microsoft Office, Clinical Trial Management System

• 14h

  Consulting Dermatologist - Central Rater & Reviewer (Canada)

  Télétravail au Canada

  TélétravailContrat

  

  Cogstate

  3+ ansCandidates need an MD or DO specializing in dermatology with an active, unrestricted medical licence and 3-5 years of post-training practice. Experience with dermatology outcome scales and telehealth and web-based clinical trial systems is required.

  Telehealth platforms, Microsoft Office, Web-based clinical trial systems

• 15h

  Supply Chain Manager - Clinical Distribution

  Mississauga, ON

  Temps plein

  A

  Astek

  3+ ansCandidates need 3 to 5 years of experience in clinical trials, logistics, warehouse operations or supply chain, plus a business, operations, supply chain or related bachelor's degree. Strong SAP skills and analytical, problem-solving abilities are required; pharmaceutical experience and APICS, SCOR, Lean or Six Sigma certifications are assets.

  SAP, IT systems, GMP systems, CAPA system

• 1j

  Nurse 2 - Operating Room

  Winnipeg, MB

  Sur place

  

  Winnipeg Regional Health Authority: The WRHA also provides health care support and specialty referral services to nearly 500,000 Manitobans who live outside its boundaries as well as…

  Winnipeg Regional Health Authority needs a graduate of an approved registered nursing program with post-basic perioperative education and a current CRNM registration. Recent operating room experience or completion of AORN Periop 101 is required, and acute care experience is preferred.

  Windows, spreadsheets, databases

• 1j

  Territory Manager

  Toronto, ON

  Temps plein

  TS

  The Stevens Company

  3+ ansCandidates need 3 to 5 years of medical device, distribution or territory sales experience and a proven record of building new business. A bachelor's degree is preferred, and Ontario healthcare market knowledge and a valid driver's licence and passport are strong assets.

  CRM

• 1j

  Agent de liaison médicale, Néphrologie / Medical Science Liaison, Nephrology

  Canada

  Temps plein

  OC

  Otsuka Canada Pharmaceutical Inc.

  3+ ansMD, Pharm. D., Ph. D. ou équivalent; 3 à 5 ans d'expérience comme agent de liaison en sciences médicales; Connaissance approfondie de la néphrologie

  Renal diseases, Literature, Research, Clinical trials, Clinical research, Ethics

16 entreprises