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Research nurse • victoriaville qc

Dernière mise à jour : il y a 7 heures
  • Offre sponsorisée
Clinical Research Associate

Clinical Research Associate

Headssaint-esprit, qc, Canada
Temps plein
Heads, a global CRO, is seeking a Clinical Research Associate (CRA) based in Canada for its growing international hematology / oncology Clinical Trials program. The CRA is responsible for ensuring tha...Voir plusDernière mise à jour : il y a 1 jour
  • Offre sponsorisée
  • Nouvelle offre
Research & Development Technologist

Research & Development Technologist

Yoplait Liberté CanadaGreater Montreal Metropolitan Area, Canada
Temps plein
Main Mission : The Dairy Research and Development Technologist, specializing in yogurt manufacturing, supports new product development activities, pilot tests, and production trials.They work under t...Voir plusDernière mise à jour : il y a 18 heures
Senior CRA / Clinical Research Associate- FSP

Senior CRA / Clinical Research Associate- FSP

ParexelRemote, Quebec, Canada
Télétravail
Temps plein
When our values align, there's no limit to what we can achieve.Parexel FSP is looking for a CRA in the Quebec Area of Canada. Cell Therapy Trial experience strongly preferred.Quebec CRA needs to be ...Voir plusDernière mise à jour : il y a 5 jours
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Clinical Data Manager / / (full-time, remote)

Clinical Data Manager / / (full-time, remote)

Everest Clinical Research.saint-valere, qc, Canada
Télétravail
Temps plein
Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device...Voir plusDernière mise à jour : il y a 22 heures
university professor

university professor

Université du Québec en Abitibi-TémiscamingueQC, CA
78 539,00 $CA – 130 062,00 $CA par an
Temps plein
Conduct research in field of specialization.Conduct seminars and discussion groups.Direct research programs of graduate students. Prepare, administer and grade assigned work.Teach one or more univer...Voir plusDernière mise à jour : il y a 5 jours
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Junior Research Analyst

Junior Research Analyst

avuasaint-esprit, qc, Canada
Temps plein
You will be responsible for conducting in-depth analysis, monitoring industry trends, and providing valuable insights to support strategic decision-making within the energy sector.The ideal candida...Voir plusDernière mise à jour : il y a 1 jour
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Product Designer

Product Designer

IFG - International Financial Groupvictoriaville, qc, Canada
128 000,00 $CA – 133 000,00 $CA par an
Temps plein
Job Title : AI Product designer.Start date : ASAP (strong potential for extension).We are looking for Product Designers with strong skills in visual design, interaction design, concepting, and protot...Voir plusDernière mise à jour : il y a 2 jours
Nurse Practitioner

Nurse Practitioner

Treasury Board of Canada SecretariatMontréal Island, Québec
84 187,00 $CA – 98 114,00 $CA par an
DND-EA-NAST-521767 National Defence.Calgary (Alberta), Cold Lake (Alberta), Edmonton (Alberta), Suffield (Alberta), Wainwright (Alberta), Comox (British Columbia), Victoria (British Columbia), Vanc...Voir plusDernière mise à jour : il y a plus de 30 jours
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Manager of Market Research and Commercial Insights

Manager of Market Research and Commercial Insights

Telnasaint-valere, qc, Canada
Temps plein
Telna is seeking an experienced and strategic Director of Market Research and Commercial Insights to lead our market research initiatives and commercial strategy development.In this role, you will ...Voir plusDernière mise à jour : il y a 17 heures
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Oncology Clinical Research Associate II - WEST CANADA (no travel)

Oncology Clinical Research Associate II - WEST CANADA (no travel)

ICON Strategic Solutionsvictoriaville, qc, Canada
Temps plein
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Works on multiple trials within Onco...Voir plusDernière mise à jour : il y a 2 jours
RN (registered nurse)

RN (registered nurse)

CISSS des LaurentidesQC, CA
35,54 $CA par heure
Temps plein +1
Registered nursing / registered nurse (RN, ASN, BSN, BScN, MSN, MScN).Registered psychiatric nurse / nursing.Registered nursing, nursing administration, nursing research and clinical nursing, other.Hos...Voir plusDernière mise à jour : il y a 12 jours
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Roster biostatistician

Roster biostatistician

Marshall Clinical Research Consulting, Incsaint-valere, qc, Canada
Temps plein
Marshall Clinical Research Consulting, Inc.The company is dedicated to providing impactful, evidence-driven results across diverse health research methodologies such as systematic reviews, clinical...Voir plusDernière mise à jour : il y a 7 heures
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Account Manager - Remote

Account Manager - Remote

Info-Tech Research Groupvictoriaville, qc, Canada
Télétravail
Temps plein
Create and execute sales and service activity plans.Manage member life-cycle tasks, including scheduling and eventually leading calls. Own all account management conversations with secondary account...Voir plusDernière mise à jour : il y a 1 jour
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Tax Litigation Lawyer

Tax Litigation Lawyer

Taxpayer Lawsaint-esprit, qc, Canada
Temps plein
Taxpayer Law specializes in tax litigation and disputes, offering expert advice to a range of clients, including business owners and individuals. Tax Litigation Lawyer at Taxpayer Law.The role invol...Voir plusDernière mise à jour : il y a 2 jours
Remote Data Research Intern

Remote Data Research Intern

FocusGroupPanelSaint-Louis-de-Gonzague, Quebec, Canada
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Remote Work From Home Data Entry Clerk for Entry Level Position.Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, wo...Voir plusDernière mise à jour : il y a 6 jours
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Senior Researcher

Senior Researcher

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Temps plein
Join as Track Chair and Showcase Your Expertise at Bentham Science Sponsored Conference - 22nd International Medicine and Biosciences Conference 2025. We are delighted to invite you to participate i...Voir plusDernière mise à jour : il y a 2 jours
Registered Nurse

Registered Nurse

Bayshore HealthCareNorthern Quebec - Remote regions, Quebec, Canada
Télétravail
Northern Quebec - Remote regions.Full time, Part-time, and Casual opportunities available.Make “being the difference” your Career at Bayshore. Bayshore is looking for caring and capable Registered N...Voir plusDernière mise à jour : il y a plus de 30 jours
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【勤務地東京】 ジュニア法人営業 / Account Manager -海外研修あり!

【勤務地東京】 ジュニア法人営業 / Account Manager -海外研修あり!

TransPerfectsaint-esprit, qc, Canada
Temps plein
OJTがございますので、新卒や営業未経験の方も安心してご応募ください。.Account Manager, Account Executive, Business Development Directorとキャリアパスが準備されており、将来的にマネジメントをお願いします。. VPとして活躍している社員もおり、年齢にとらわれず「頑張った人が適正に評価される」環境がグローバル全体で整っています。.S...Voir plusDernière mise à jour : il y a 2 jours
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Head of Finance (Research / Contract)

Head of Finance (Research / Contract)

Ripplingsaint-esprit, qc, Canada
200,00 $CA par jour
Temps plein
This is an open freelance role to share your feedback.We are looking for feedback from Finance Leaders on our product as we expand in Canada. This is a compensated research hourly research role in e...Voir plusDernière mise à jour : il y a 2 jours
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Clinical Research Associate / Project Supervisor (French Speaker)

Clinical Research Associate / Project Supervisor (French Speaker)

Tigermedsaint-valere, qc, Canada
Temps plein
This Positions is a mixed Role of CRA and Project Supervisor.This position is responsible for project management and study site management from site selection to initiation until monitoring and clo...Voir plusDernière mise à jour : il y a 2 jours
Clinical Research Associate

Clinical Research Associate

Headssaint-esprit, qc, Canada
Il y a 1 jour
Type de contrat
  • Temps plein
Description de poste

Heads, a global CRO, is seeking a Clinical Research Associate (CRA) based in Canada for its growing international hematology / oncology Clinical Trials program.

This is a full-time job.

Job overview :

The CRA is responsible for ensuring that the conduct of a clinical trial at selected Investigational Sites is according to the currently approved protocol / amendments, ICH GCP guidelines, the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations.

He / she is the primary responsible person for communication on operational study related activities between the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships.

The most important responsibility is to ensure that the subjects’ rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents.

Main responsibilities :

  • Acknowledges, follows& ensures compliance with the Company’s Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above
  • In case of deviation from the approved protocol, ICH GCP guidelines and / or applicable legislation during the study conduct, the CRA is responsible for reporting it to the Line Manager and other applicable roles according to SOPs
  • Conducts pre-study visits at potential investigational sites, to perform the study related feasibility and / or selection activities and evaluate their resources and facilities
  • Collaborates with the Regulatory Affairs Department and concerned Clinical Operations staff for clinical submissions and contracts respectively for :
  • Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome
  • Preparation of study contracts & relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation
  • Fully explains the purposes, set-up, and procedures of the clinical trial to the Investigators and is responsible for training and assisting them in the conduct of clinical trials
  • Prepares and updates the Clinical Trial Files throughout the study and ensures the proper collection of essential documents and other study-related documents during the trial
  • Ensures that the Sites are supplied with adequate study medication, verifies that drug accountability is performed correctly and ensures the drug’s safe shipment, storage, dispensing, return and destruction, as applicable
  • The CRA is responsible for adequate monitoring of the clinical trial conduct at the Investigational Sites (e.g., performs monitoring visits at the Sites) during which he / she :
  • Ensures Investigators’ knowledge and compliance with the clinical protocol and ICH GCP guidelines
  • Verifies that Investigators’ qualifications and resources remain adequate throughout the trial period
  • Reviews and verifies the data reported in the eCRF against source data, according to the monitoring plan which determines the depth and extend of source data verification
  • Ensures that written informed consent has been obtained from all subjects prior to any study related screening activity or requirement
  • Fully verifies subject consent procedures against ICH GCP guidelines and legislation
  • Checks and discusses recruitment and timelines with the Investigators
  • Checks the storage and adequacy of clinical trial supplies
  • Maintains and updates the Investigator’s Files as required to confirm completeness
  • Co-ordinates the proper reporting of Safety Information to the Sponsor according to the Safety Reporting Plan, where applicable. CRA is also responsible for making sure that the Investigators are adequately trained in identifying and reporting AEs / SAEs
  • Checks that all submissions, reports, notifications and applications to the IEC / IRB or Regulatory Authorities have been made by the Investigator in a timely manner
  • Performs drug accountability and ensures the proper dispensing of study drug to the patient
  • Prepares reports to document all discussions, measures and actions made during a monitoring visit, telephone contact or remote monitoring. The CRA also sends summary of these reports to the Investigators
  • Participates in study specific conference calls and meetings to review progress of ongoing clinical trials; provides feedback to the CRA Manager
  • In case of an audit or regulatory inspection, the CRA is responsible for informing and preparing the Site and facilitating the procedure. The CRA works with the appropriate study team members and Quality (QA) in order the corrective actions are in place and performed as soon as possible
  • Collaborates with the CRA Manager and Clinical Operations Manager to develop feasibility evaluation questionnaires, contact the Investigators to collect feasibility-related information, perform site screening and selection
  • Supports financial issues of the study, including Investigators’ payments
  • Manages timely subject enrolment and quality data collection
  • Ensures that procedures are in place for appropriate optimization of patients into the study : evaluates patients’ recruitment and determines if it is according to the operational plan & patients’ target
  • Closes down study sites on completion of the trial
  • Participates in departmental planning sessions, and SOP development, if required
  • Provides coaching, mentoring and management to the newly appointed and / or inexperienced CRAs to ensure that their role and contribution is optimized

Job Requirements :

  • Bachelor’s and / or master’s degree (preferably in Health Sciences)
  • Previous Work Experience desirable :
  • 6-12 months’ work experience as a CRA
  • Excellent command of English and French both oral and written
  • Attendance of an ICH GCP training course (desirable)
  • Good computer skills
  • Good general communication skills
  • Good organizational skills
  • Ability to work independently and be a good team player at the same time
  • Ability to communicate diplomatically, but also effectively with study Site personnel
  • Ability to deal adequately with stressful situations, flexible timelines and work pressure
  • Ability to maintain complete overview and deal with several issues at the same time
  • Ability to work according to specific SOPs, guidelines, regulations & ethical principles in the daily practice
  • Ability for frequent international and local travelling, including evenings and overnight stays
  • Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.

    Competitive remuneration package comes on top.

    In Heads we consider Data Protection an integral part of our operational business principles and are committed to respecting your privacy. For information on how we process your personal data please visit our Privacy Notice to Candidates :