Emplois “Clinical research” au Canada – Page 4

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• 29j

  Clinical Research Associate II/Senior CRA - French Fluency

  Télétravail au Canada

  TélétravailTemps plein

  PR

  Premier Research International LLC

  4+ ansCandidates need an undergraduate degree (or equivalent) and at least 4 years of on-site clinical research monitoring experience, plus French fluency and a base in Quebec. Strong customer focus, a valid driver's licence and the ability to travel 8-10 monitoring visits per month are also required.

  Clinical research, Research, Monitor activities, Clinical trials, Google Cloud, DOS

• 1 mois

  Senior Clinical Research Associate

  Burlington, ON +3

  Sur placeTemps plein

  IC

  ICR Canada - CAN

  3+ ansCandidates need a bachelor's degree or equivalent in a scientific or health field, plus at least 3 years of clinical monitoring experience for this senior level. Knowledge of ICH and regulatory rules for drug trials and fluent English and French are required.

  Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

• 1 mois

  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

  1 mois

  Clinical Research Coordinator

  Stoney Creek, ON

  Temps plein

  

  ClinSurge Research

  Candidates need a bachelor's degree in health sciences, life sciences, nursing or a related field, plus phlebotomy certification and strong knowledge of GCP, Health Canada and IRB rules. Clinical research experience of 1-3 years is preferred, along with strong organizational and communication skills.

  Medidata, RAVE, Microsoft Office, electronic data capture (EDC) systems

  1 mois

  Clinical Research Coordinator

  Nepean, ON

  Temps plein

  

  ClinSurge Research

  Candidates need a bachelor's degree in health sciences, life sciences, nursing or a related field, plus phlebotomy certification and strong knowledge of GCP, Health Canada and IRB rules. Clinical research experience of 1-3 years is preferred, along with strong organizational and communication skills.

  Medidata, RAVE, Microsoft Office, electronic data capture (EDC) systems

• 1 mois

  Clinical Research Assistant (SRI) - Physical Sciences - Regular Full-time 2025-15682

  Toronto, ON

  Temps plein

  SH

  Sunnybrook Health Sciences Centre

  Candidates need an M.Sc or Ph.D. in biomedical or related sciences, experience with imaging methods and image analysis, and knowledge of research regulations. Strong organization, communication and attention to detail are also required.

  Clinical research, Research, Time management, Organizational skills, Communication skills, Attention to detail

• 1 mois

  Director of Clinical Research

  Toronto, ON

  TélétravailTemps plein

  

  Tiny Health

  6+ ansCandidates need a PhD, MD, MS/MPH or equivalent in a life science or clinical field, plus 6+ years of clinical research experience. They must have designed human clinical studies, handled IRB submissions and led cross-functional teams.

  Shotgun metagenomics, Slack

• 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

  Study Coordinator - Clinical Research

  Toronto, ON

  50k–55k $/anTemps plein

  

  Pharma Medica Research Inc.

  1+ ansCandidates need a B.Sc. with one year of clinical trial experience, or an M.Sc. with adequate clinical trial knowledge. They also need Phase I protocol knowledge, GCP training, strong English communication and organizational skills, and the ability to work in a Canadian-eligible role.

  computer software applications

• 1 mois

  Clinical Research Lead

  Vancouver, BC

  Temps plein

  

  MetaOptima: MetaOptima is a digital health tech company dedicated to revolutionizing the dermatology and skin care industry with affordable, effective and…

  Candidates need a bachelor's degree in a health, life science or related field, or equivalent experience. They need hands-on experience across the clinical study lifecycle, knowledge of Good Clinical Practice and ethics, and the ability to manage several studies while personally writing and reviewing study documents.

  Clinical research, Prepare building site, Recruitment, Reporting, Research, Documentation

• 1 mois

  Senior Budget Specialist, Clinical Research

  Waterloo, ON

  Temps plein

  

  Probity Medical Research Inc

  5+ ansCandidates need a bachelor's degree or college diploma in finance, business, accounting, economics, life sciences or a related field, plus at least 5 years of clinical trial budget experience. Strong negotiation, financial analysis and Microsoft Office skills are essential.

  Microsoft Excel, Microsoft Word, DocuSign, PDF editing software

  1 mois

  Senior Contract Specialist, Clinical Research

  Waterloo, ON

  Temps plein

  

  Probity Medical Research Inc

  5+ ansCandidates need a bachelor's degree or college diploma in law, business, economics or a related field, and at least 5 years of contract management or clinical research contract experience. Strong negotiation, Microsoft Office and DocuSign skills are required, and candidates must handle confidential documents with discretion.

  Microsoft Word, Microsoft Excel, DocuSign, PDF editing software, contract management systems

  1 mois

  Budget Specialist, Clinical Research

  Waterloo, ON

  Temps plein

  

  Probity Medical Research Inc

  1+ ansCandidates need a bachelor's degree or college diploma in clinical research, health or life sciences, and at least 1 year as an on-site clinical research coordinator or assistant, or 2 years in on-site clinical research administration. Budget negotiation experience, strong Excel skills and DocuSign and PDF software experience are needed.

  Microsoft Excel, DocuSign, PDF software, KPI tracker

  1 mois

  Contract Specialist, Clinical Research

  Waterloo, ON

  Temps plein

  

  Probity Medical Research Inc

  1+ ansCandidates need a business, legal, life sciences or related diploma or degree, and one to three years in clinical research or another regulated environment. They should work well within SOPs, be detail-oriented, and handle many deadlines at once.

  Microsoft Word, Microsoft Excel, Microsoft Outlook, DocuSign

  1 mois

  Recruitment Specialist, Clinical Research

  Waterloo, ON

  Temps plein

  

  Probity Medical Research Inc

  1+ ansCandidates need at least one year in a healthcare or research customer-facing role and at least one year creating qualification assessments and tracking call center metrics. A college diploma in healthcare, life sciences or a related field is preferred, along with strong computer, communication and documentation skills.

  MS Office, Excel, EDC systems, clinical trial management software, CRM

• 1 mois

  Clinical Research Assistant

  Markham, ON

  Temps plein

  

  Everest New

  Candidates need a bachelor's degree in clinical, medical or life sciences, with M.Sc. or higher preferred. Experience with Phase I through IV clinical trials, knowledge of drug and device regulations, strong written communication and Microsoft Office skills are needed.

  Microsoft Office, clinical data capture system

  1 mois

  Clinical Research Safety Associate

  Markham, ON

  TélétravailTemps plein

  

  Everest New

  2+ ansEverest New needs candidates with a master's or PhD in a clinical or health field and at least two years of clinical research experience across Phase I to IV trials. Strong written and verbal communication, organization and confidentiality are required, with experience in a clinical data capture system and MS Office preferred.

  MS Office, clinical data capture system

• 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

  Clinical Research Technician

  Montréal, QC +1

  Sur placeTemps partiel

  

  Altasciences Company Inc

  Altasciences needs a high school diploma or a health-related diploma, plus excellent French and English communication and a customer service focus. Knowing another language is an asset, and the role suits people who work well in a fast-paced setting.

  Clinical research, Regulatory compliance, Google Cloud, Confidentiality, Customer service, Operations management

  1 mois

  Clinical Research Nurse

  Montréal, QC +1

  Sur placeTemps plein

  

  Altasciences Company Inc

  Altasciences needs a registered nurse with a DEC and OIIQ permit, good French and English, strong communication skills, and the ability to handle several priorities in a fast-paced setting. Microsoft Office knowledge and clinical research experience are an asset.

  emergency crash cart

• 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 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

  1 mois

  Experienced Clinical Research Associate - Sponsor Dedicated

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Candidates need a bachelor's degree or RN in a related field, knowledge of Good Clinical Practice and ICH guidelines, good computer skills, and strong communication skills. Travel of up to 75% on a regular basis is required.

  Electronic data capture systems, Tracking systems

• 1 mois

  Clinical Research Manager- FSP

  Quebec

  Télétravail

  PI

  Parexel International (Canada) LTD

  5+ ansCandidates need five to six years of clinical research experience, ideally as a CRA, with strong project management and clinical trial knowledge. A bachelor's degree in science is required, and an advanced degree is preferred.

  CTMS, eTMF

14 entreprises