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Clinical research • drummondville qc

Dernière mise à jour : il y a 13 heures
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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 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 4 jours
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Oncology Clinical Research Associate II - WEST CANADA (no travel)

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

ICON Strategic Solutionsdrummondville, 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 1 jour
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Regulatory Affairs Manager (Part-Time, Canada Based)

Regulatory Affairs Manager (Part-Time, Canada Based)

Advanced Clinicaldrummondville, qc, Canada
Temps partiel
Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the ...Voir plusDernière mise à jour : il y a 1 jour
Specialist I, Clinical Solutions - SCI

Specialist I, Clinical Solutions - SCI

SysmexQC, CA
70 200,00 $CA par an
This is the time to let your talent come to life.To maximize your knowledge and use it for the greater good.To work with the best professionals using state-of-the-art technology, and improve lives ...Voir plusDernière mise à jour : il y a plus de 30 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 13 heures
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Research & Development Technologist

Research & Development Technologist

Yoplait Liberté CanadaGreater Montreal Metropolitan Area, Canada
Temps plein
The Dairy Research and Development Technologist, specializing in yogurt manufacturing, supports new product development activities, pilot tests, and production trials. They work under the supervisio...Voir plusDernière mise à jour : il y a 1 jour
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Clinical Business Analyst

Clinical Business Analyst

Tek Leaders Incsaint-esprit, qc, Canada
Temps plein
Role : Technical Clinical System Analyst – Healthcare (Utilization Management).Type of Hire - Contract / C2H : Contract.We are seeking a Technical Clinical Analyst with expertise in Clinical Utilizati...Voir plusDernière mise à jour : il y a 1 jour
Planning, Programming And Research Officer

Planning, Programming And Research Officer

Cree Board of Health and Social Services of James Bay (CBHSSJB)Nord-Du-Québec, Canada, CA
Temps plein
SUMMARY OF THE POSITIONPerson who is responsible for one or more programs with a view to providing professional assistance for the development of services. She / he conducts research activities that a...Voir plusDernière mise à jour : il y a 4 jours
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Clinical Specialist

Clinical Specialist

Medtronicsaint-esprit, qc, Canada
Temps plein
At Medtronic, you can begin a lifelong career focused on research and innovation, championing equity and access to healthcare for all. Your leadership will make an impact, removing barriers to drive...Voir plusDernière mise à jour : il y a 1 jour
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Clinical Database Developer

Clinical Database Developer

Planet Pharmasaint-esprit, qc, Canada
CDI
We are currently partnered with one of our leading global health care clients who are seeking Clinical Database Developer on a remote basis in Canada. Develops programming / configuration of Veeva and...Voir plusDernière mise à jour : il y a 1 jour
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Manager of Market Research and Commercial Insights

Manager of Market Research and Commercial Insights

Telnadrummondville, 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 1 jour
Remote Data Research Intern

Remote Data Research Intern

FocusGroupPanelSaint-Louis-de-Gonzague, Quebec, Canada
Télétravail
Temps plein +1
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 5 jours
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Clinical Data Manager / / (full-time, remote)

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

Everest Clinical Research.drummondville, 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 1 jour
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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 1 jour
Senior Clinical Project Manager.

Senior Clinical Project Manager.

PSIGreater Montreal Area, QUEBEC, CA
38,79 $CA –48,48 $CA par heure
Management of medium-sized (5-15 countries and / or full service) or large (> .Adherence to and promotion of principles of delivery and service in dealing with PSI customers.Project Supervision of sma...Voir plusDernière mise à jour : il y a plus de 30 jours
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Lead Clinical Data Manager

Lead Clinical Data Manager

Warman O'Briendrummondville, qc, Canada
Temps plein
Senior Clinical Data Manager | Global CRO | Full Time | Remote North America.Our client is a well-established mid-sized CRO based in the Toronto Area and known for providing top-notch clinical solu...Voir plusDernière mise à jour : il y a 1 jour
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RFR-CIS-060 - Clinical Informatics Specialist

RFR-CIS-060 - Clinical Informatics Specialist

Amyanteksaint-esprit, qc, Canada
Temps plein
RFR-CIS-060 - Clinical Informatics Specialist.Services will be performed via remote access.Services shall not be performed remotely from outside of Canada. Degree or Diploma in healthcare informatic...Voir plusDernière mise à jour : il y a 1 jour
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Clinical Research Associate / Project Supervisor (French Speaker)

Clinical Research Associate / Project Supervisor (French Speaker)

Tigermeddrummondville, 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 1 jour
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Senior Clinical Data Manager

Senior Clinical Data Manager

Saint Laurent Consultingdrummondville, qc, Canada
Temps plein
On behalf of our client, Saint Laurent Consulting is hiring a Senior Clinical Data Manager.This role involves leading clinical data management activities for various projects, ensuring data integri...Voir plusDernière mise à jour : il y a 1 jour
Clinical Research Associate

Clinical Research Associate

Headssaint-esprit, qc, Canada
Il y a 18 heures
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 :