Emplois “clinical trial systems” au Canada – Page 28

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• 1 mois

  Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)

  Québec, QC +1

  TélétravailTemps plein

  WC

  Worldwide Clinical Trials Holdings, Inc.

  5+ ansWorldwide Clinical Trials Holdings, Inc. needs candidates with 5+ years as a Clinical Research Associate, oncology experience, a 4-year degree or nursing degree, and fluent written and spoken English and French. Candidates must live in Canada.

  Microsoft Office, CTMS, EDC systems

• 1 mois

  Director, Regulatory Pre-Award Strategy - Europe/Canada- Remote

  Manitoba +5

  TélétravailTemps plein

  WC

  Worldwide Clinical Trials Limited

  12+ ans3+ gestionCandidates need at least twelve years of global clinical pharmaceutical experience, including three years managing global teams, and strong Regulatory Affairs experience. A life science degree or equivalent is preferred, along with fluency in English and the local office language.

  Leadership, Presentation skills, Team leadership, Sales, Project management, Coaching

• 1 mois

  Manager, Patient Advocacy

  Montréal, QC

  Temps plein

  BC

  BMS Canada Company

  7+ ansBachelor's degree in communications, public relations, public affairs, business or sciences; Minimum 7 years of stakeholder engagement or communications experience; Fluency in English and French, written and verbal

  Communication skills, Stakeholder management, Leadership, Regulatory compliance, Public relations, Project management

• 1 mois

  Medical Equipment and Systems Specialist

  Montréal, QC +1

  Sur placeTemps plein

  

  Altasciences Company Inc

  1+ ansCandidates need a high school diploma, about one year of related experience, and strong computer skills in Microsoft Office. Bilingual English and French is required for Canadian locations, along with strong technical reading and written communication.

  eSource system

• 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

  1 mois

  Sr CTM

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  Syneos Health needs candidates with a bachelor's degree or RN in a related field, demonstrated site management and monitoring expertise, and knowledge of GCP and ICH guidelines. Strong leadership, conflict resolution, budget and computer skills are also required.

  CTMS, EDC, eDiary, ePROs, Trial Master File (TMF), IVRS/IWRS

  1 mois

  Real World Biostatistician - RWE Cardiometabolic experience (hiring in Canada and US) PhD mandatory

  Télétravail au Canada

  TélétravailTemps plein

  

  Syneos Health, LLC

  5+ ansCandidates need a master's or PhD in biostatistics, statistics, epidemiology or a related field, plus 5+ years of real-world data analytics. They need SAS, R or Python, SQL and OMOP knowledge, and experience with observational study design and causal inference.

  SAS, R, Python, SQL, OMOP, ICD

  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

  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

  1 mois

  Site Activation Specialist II Remote in Canada-QC-Montreal (Client Dedicated)

  Montréal, QC

  TélétravailTemps plein

  SH

  Syneos Health Canada LP

  Syneos Health Canada LP needs a bachelor's degree, detailed knowledge of clinical trial processes across Phases II to IV and ICH GCP, and clinical trial start-up experience. Candidates must be fluent in French and English and able to negotiate, manage vendors and handle multiple budgets.

  Regulatory compliance, Process improvement, Communication skills, SAM, Data protection, Quality control

• 1 mois

  Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have (EMEA /LATAM/Canada)

  Télétravail au Canada

  TélétravailTemps plein

  IH

  inVentiv Health Clinical Mexico, S.A. de C.V.

  Syneos Health needs candidates with regulatory submission experience, including small molecule CMC and Veeva RIM. Strong leadership, client-facing and dossier-writing skills are needed, plus knowledge of EMEA, LATAM and Canadian regulatory requirements.

  Veeva RIM

• 1 mois

  Medical Science Liaison, Dermatology (Central)

  Ontario

  TélétravailTemps plein

  C3

  CAN - 3032 Takeda Canada Inc.

  5+ ansCandidates need an MD, PharmD or PhD, at least 5 years of pharmaceutical industry or clinical experience, and strong scientific communication skills. Dermatology experience, French bilingualism and willingness to travel are assets.

  Microsoft Office, Microsoft Teams, CRM

• 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

11 entreprises