Emplois “Clinical trials management system” au Canada – Page 20

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• 1 mois

  CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada

  Toronto, ON +1

  TélétravailTemps plein

  FF

  FTCAN Fortrea Canada Inc.

  1+ ansCandidates need a university, college or allied health degree (such as nursing licensure) and one to three or more years of clinical monitoring experience. Oncology or ophthalmology experience and French language skills are preferred.

  Fortrea data management systems

  1 mois

  Clinical Operations Manager (COM) - Montreal, Canada - Hybrid

  Montréal, QC

  TélétravailTemps plein

  FF

  FTCAN Fortrea Canada Inc.

  4+ ansCandidates need 4-6 years of clinical research experience, a life science or health degree (or equivalent experience), and knowledge of ICH, GCP and FDA rules. Fluency in French and English, strong organization and the ability to lead junior staff are also needed.

  clinical systems, regulatory systems, finance systems

• 1 mois

  Clinical Trial Manager

  Télétravail au Canada

  TélétravailTemps plein

  FF

  FTINC Fortrea Inc.

  4+ ansCandidates need a life science degree or allied health certification, four or more years of clinical research experience, and knowledge of GCP, ICH and regulatory guidelines. Fluent English and skill with Microsoft Office, EDC, CTMS and eTMF systems are also required.

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

• 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

  1 mois

  Clinical Operations Manager-FSP

  Quebec

  TélétravailTemps plein

  PI

  Parexel International (Canada) LTD

  Candidates need strong organizational and budget and contract negotiation skills, a solid understanding of the local regulatory environment, and knowledge of ICH/GCP. They must lead and influence teams and sites, and work effectively in a remote virtual environment.

  Clinical trials, COM, R, Regulatory compliance, Google Cloud, Reporting

  1 mois

  Local Study Associate Director- FSP

  Ontario

  Télétravail

  PI

  Parexel International (Canada) LTD

  3+ ansCandidates need at least 3 years in clinical development operations such as CRA or Senior CRA work, plus strong knowledge of ICH-GCP and Canadian regulations. Oncology experience is required, cell therapy is strongly preferred, and a life science bachelor's degree is expected.

  CTMS, eTMF

  1 mois

  Clinical Trial Coordinator- Finance- FSP

  Quebec

  Télétravail

  PI

  Parexel International (Canada) LTD

  1+ ansParexel needs candidates with one to two years in clinical research or healthcare, a life sciences or equivalent background, and budget negotiation experience. Candidates should know Good Clinical Practice and Good Documentation Practice, and be strong in Microsoft Excel and fluent in English and French.

  CTMS, eTMF

  1 mois

  Global Site Start Up Lead - FSP

  Ontario

  Télétravail

  PI

  Parexel International (Canada) LTD

  4+ ansCandidates need 4-6 years of clinical drug development experience with study start-up, vendor management, and knowledge of ICH/GCP. Strong leadership, negotiation, data-driven planning and proficiency with CTMS, TMF and Microsoft Office are required.

  CTMS, TMF

  1 mois

  Site Activation Partner/Study Start Up Specialist - FSP

  Alberta +3

  Télétravail

  PI

  Parexel International (Canada) LTD

  2+ ansParexel International asks for at least 2 years of clinical trial site activation experience, knowledge of ICH/GCP, FDA and local regulations, and fluency in English and a local language. A life sciences bachelor's degree is preferred.

  Clinical trials, Regulatory compliance, Pharmaceutical industry, Google Cloud

• 1 mois

  Quality Assurance Supervisor

  Strathroy, ON

  Temps plein

  CC

  Catalent Company

  3+ ans1+ gestionCandidates need a bachelor's degree in science or engineering, 3+ years of QA/QC experience, and ideally supervisory experience. Experience in GMP or pharmaceutical manufacturing is preferred.

  Quality assurance, Regulatory compliance, Production processes, Quality control systems, Process improvement, Documentation

  1 mois

  Quality Management System Specialist

  Strathroy, ON

  Temps plein

  CC

  Catalent Company

  2+ ansCandidates need a diploma or bachelor's degree in life science or a related field and at least 2 years in quality or operations. Experience in a regulated manufacturing environment is required, with pharmaceutical quality management experience and FDA or Health Canada inspection exposure preferred.

  Microsoft Office Suite, Outlook, Excel, PowerPoint, Word

  1 mois

  Director of Quality

  Strathroy, ON

  Temps plein

  CC

  Catalent Company

  7+ ansCandidates need a science or technical bachelor's degree and 7+ years of leadership experience in a GMP manufacturing or pharmaceutical setting. They must have hands-on experience hosting and managing FDA and HPFB inspections, and strong communication and Microsoft Office skills.

  Microsoft Outlook, Microsoft Excel, Microsoft Access, Microsoft Word

• 1 mois

  Medical Director, Oncology Clinical Development - Hematology

  Mississauga, ON

  TélétravailTemps plein

  GS

  GlaxoSmithKline Services Unlimited

  Candidates need an MD with board certification or eligibility in oncology or hematology, including experience treating clonal myeloid disorders. Experience in clinical trial conduct, medical monitoring and GCP/ICH-compliant drug development is required.

  Monitor activities, Regulatory compliance, Decision making, Collaboration, Hazard assessment, Google Cloud

• 1 mois

  Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

  Mississauga, ON

  TélétravailTemps plein

  GL

  GlaxoSmithKline LLC

  Candidates need an MD with board certification or eligibility in oncology, haematology or a related specialty. They also need clinical trial experience in oncology, including medical monitoring and safety review, and experience working in cross-functional matrix teams.

  Monitor activities, Regulatory compliance, Decision making, Collaboration, Hazard assessment, Google Cloud

• 1 mois

  PRODUCTION SHIFT MANAGER (Afternoon/Evening Shift)

  Aurora, ON

  Temps plein

  PH

  Piramal Healthcare (Canada) Limited

  Candidates need experience leading pharmaceutical or regulated manufacturing, knowledge of cGMP, GDP and safety standards, and skills in team leadership, root cause analysis and lean or Six Sigma methods.

  Good manufacturing practices, Documentation, Housekeeping, Cleaning, Root cause analysis, Scheduling

• 1 mois

  Sr. Project Manager, Quality Assurance (QA)

  Burnaby, BC

  102k–135k $/anTemps plein

  EC

  Evonik Canada Inc._11

  10+ ans2+ gestionCandidates need a bachelor's degree in a science or engineering field and ten to twelve years of pharmaceutical or biopharmaceutical QA/QC experience, including at least two years in leadership. Strong cGMP knowledge, experience hosting regulatory inspections and advanced problem-solving and communication skills are required.

  Word, Excel, Access

  1 mois

  QC Specialist

  Burnaby, BC

  78k–104k $/anTemps plein

  EC

  Evonik Canada Inc._11

  5+ ansCandidates need a BSc or MSc in chemistry, biochemistry, microbiology or a related science, plus about 5 to 8 years in parenteral pharmaceutical or biopharmaceutical work. QC experience, project management and strong organization and communication skills are preferred.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Visio, QC system

  1 mois

  Associate Director Engineering (Director)

  Burnaby, BC

  121k–161k $/anTemps plein

  EC

  Evonik Canada Inc._11

  10+ ansCandidates need a bachelor's degree in an technical field such as chemical engineering, and at least 10 years of engineering experience, ideally in pharmaceutical or biotech manufacturing. Strong leadership, budgeting, GMP knowledge and English communication are required.

  Clinical trials, Chemical engineering, Biotechnology, Process engineering, Budget management, Good manufacturing practices

• 1 mois

  Medical Science Liaison - Pharma (Montreal)

  Télétravail au Canada

  TélétravailTemps plein

  AC

  Alcon Canada Inc. Company

  7+ ansBachelor's degree or equivalent directly related experience; Advanced English and French, written and verbal; About 7 years of relevant experience

  Research, Clinical trials, Market analysis, Sales, Regulatory affairs, Regulatory compliance

• 1 mois

  Chef d'équipe données senior, Senior Data Team Lead

  Montréal, 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…

  7+ ans5+ gestionBaccalauréat en sciences de la vie, santé, clinique, biologie ou mathématiques; Au moins 7 ans d'expérience en gestion de données cliniques; 5 ans minimum à un poste de responsable de la gestion des données cliniques

  Medidata Rave, Oracle InForm, EDC systems

  1 mois

  Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech

  Kirkland, QC +2

  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…

  1+ ansBilingue français-anglais (obligatoire); Baccalauréat requis, de préférence en sciences de la vie; Au moins 1 an d'expérience en suivi sur place (requis)

  EDC systems

• 1 mois

  Gestionnaire de l’activation des sites/ Site Activation Manager

  Mississauga, ON +2

  Temps plein

  IR

  IQVIA RDS Canada West ULC.

  5+ ans2+ gestionBaccalauréat en sciences de la vie ou domaine connexe (exigé); Minimum de 5 ans d'expérience, dont 2 ans en leadership (exigé); Expérience internationale démontrée (exigé)

  Outils de suivi de projet, Échéanciers et plans de projet, Bases de données internes

• 1 mois

  Clinical Trial Manager

  Montréal, QC

  HybrideTemps plein

  IC

  ICR Canada - CAN

  5+ ansCandidates need a bachelor's degree in business, finance, life sciences or a related health field, plus about 5 years of clinical research or combined clinical research and finance experience. Strong French and English communication, budget and contract negotiation skills, and solid knowledge of the local regulatory environment are required.

  clinical trial systems, finance systems

• 1 mois

  Postdoctoral Research Fellow

  Vancouver, BC

  55k $/anTemps plein

  UT

  UBC The University of British Columbia

  Candidates need a PhD from the last 5 years in computer science, data science, computational biology or a related field. They need strong Python, FastAPI and PostgreSQL skills, hands-on work with LLMs, vector databases and NLP, and experience running AWS and Docker pipelines.

  Python, FastAPI, PostgreSQL, Pinecone, Docker, AWS

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