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Research nurse Jobs in Blainville, QC

Last updated: 5 hours ago
Senior CRA / Clinical Research Associate- FSP

Senior CRA / Clinical Research Associate- FSP

ParexelRemote, Quebec, Canada
Remote
When our values align, there's no limit to what we can achieve.Parexel FSP is looking for a CRA in the Ontario and Quebec Area of Canada. Cell Therapy Trial experience strongly preferred.The Clinica...Show moreLast updated: 30+ days ago
European Nurses for VIP Client in a Private Yacht

European Nurses for VIP Client in a Private Yacht

European Nurse RecruitmentCabra, CO, es
Full-time
Quick Apply
VIP client traveling internationally aboard a luxury private yacht.This exclusive role offers a unique chance to combine your professional expertise with the excitement of exploring stunning destin...Show moreLast updated: 8 days ago
  • Promoted
Remote – No Experience Product Tester

Remote – No Experience Product Tester

OCPASaint-Jérôme, Quebec, CA
CA$45.00 hourly
Remote
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies. We guarantee 15-25 hours per week with an hourly pay of bet...Show moreLast updated: 30+ days ago
Customer Service Representative - Remote

Customer Service Representative - Remote

Toward Jobs OnlineQuebec, CA
Remote
Full-time +1
Work from Home Survey Taker (Side Gig) We are looking for people who are motivated to participate in paid research across the country and local areas. Join this Work from Home Canada Market Res...Show moreLast updated: 30+ days ago
  • Promoted
  • New!
FSP Manager, Clinical Operations- Quebec

FSP Manager, Clinical Operations- Quebec

Thermo Fisher ScientificNot Specified, QC, Canada
Full-time
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.Join our colleagues in bringing our Mission to life - enabling our customers to make the ...Show moreLast updated: 5 hours ago
Registered Nurse (RN) - Rigaud

Registered Nurse (RN) - Rigaud

RhynoCareRigaud, Ontario, Canada
Full-time
LOCAL CANDIDATES ONLY • • •.Must be fluent in English & French •.We are seeking Registered Nurses (RNs) to start work as soon as possible in the Hawkesbury-area.Shifts would be early morn...Show moreLast updated: 30+ days ago
Neighborhood Health Team Lead Nurse

Neighborhood Health Team Lead Nurse

Bayshore HealthCareChomedy / Ste-Dorothe, Quebec, Canada
Neighborhood Health Team Lead Nurse.Variety of patient care settings.Permanent and Full time opportunities available.Do you LOVE working independently with clients in the community?.Do you have a k...Show moreLast updated: 19 days ago
Research Advisor

Research Advisor

Cuso InternationalLaval, QC, CA
Full-time
This Volunteer Placement is Located in : .Please submit a Spanish Resume and Statement of Interest.Eligibility : Open to Canadian Citizens and Permanent Residents of Canada only.This is your opportuni...Show moreLast updated: 30+ days ago
Research Assistant, R&D

Research Assistant, R&D

CIRION BioPharma ResearchLaval, Canada
CA$47,320.00–CA$87,887.80 yearly
Description Research Assistant, R&D (RH2024-003)Location : Laval, Canada CIRION BioPharma Research is looking for a Research Assistant. Under the supervision of the Director, Research and Development...Show moreLast updated: 30+ days ago
  • New!
Senior Marketing Analyst, Customer Experience & Insights

Senior Marketing Analyst, Customer Experience & Insights

Intact Financial CorporationLaval, Quebec, Canada
Full-time +1
Our employees are at the heart of what we do best : helping people, businesses and society prosper in good times and be resilient in bad times. When you join our team, you're bringing this purpose to...Show moreLast updated: 12 hours ago
Infirmier (ère) / Nurse (Tusaajiapik)

Infirmier (ère) / Nurse (Tusaajiapik)

CSTUQC, CA
CA$1,552.13 weekly
Le Centre de santé Tulattavik de L’Ungava est situé à Kuujjuaq.Il dispense l’ensemble des services de santé et services sociaux dans la partie est du Nunavik. Il dessert sept communautés Inuites ave...Show moreLast updated: 30+ days ago
Nurse Practitioner

Nurse Practitioner

Treasury Board of Canada SecretariatMontréal Island, Québec
CA$84,187.00–CA$98,114.00 yearly
DND-EA-NAST-521767 National Defence.Calgary (Alberta), Cold Lake (Alberta), Edmonton (Alberta), Suffield (Alberta), Wainwright (Alberta), Comox (British Columbia), Victoria (British Columbia), Vanc...Show moreLast updated: 30+ days ago
writer

writer

4355768 Canada Inc.QC, CA
CA$28.57–CA$32.96 hourly
Permanent
Education : College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years.Experience : 1 year to less than 2 years. Advertising, marketing and public relations agen...Show moreLast updated: 5 days ago
LIMS Logistics Specialist

LIMS Logistics Specialist

Planet TechnologyLaval, QC, CA
LIMS Logistics Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite LIMS Logistics Specialist with 2+ years’ experience working within Clinical ...Show moreLast updated: 30+ days ago
Oncology Clinical Research Associate - Canada -

Oncology Clinical Research Associate - Canada -

ScimegaLaval, Quebec
CA$46,147.00 yearly
Under the direction of the Director, Clinical and Scientific Affairs, the CTL is responsible for execution of clinical trials, from the site selection, start-up and enrollment phases up to the stud...Show moreLast updated: 30+ days ago
  • Promoted
Executive Assistant

Executive Assistant

Groupe ParimaLaval, Quebec
Quick Apply
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994.For over 25 years, we have developed expertise in the development and manufacturing of non-sterile...Show moreLast updated: 30+ days ago
  • Promoted
Remote Work From Home Online - Paid Research Panelist - Data Entry Clerk Welcome

Remote Work From Home Online - Paid Research Panelist - Data Entry Clerk Welcome

Apex Focus GroupLaval, Quebec, Canada
CA$850.00 weekly
Remote
Remote Work From Home Online Paid Research Panelist PartTime Data Entry Clerk Welcome.Our company is looking for qualified candidates to take part in paid national and local focus groups clinical...Show moreLast updated: 30+ days ago
Auxiliary nurse

Auxiliary nurse

Cogir ImmobilierSaint-Eustache
CA$22.50–CA$23.77 hourly
Part-time
Every day, our team of enthusiasts makes a difference to residents.The relationship of “human for human” is at the heart of our approach and corporate philosophy. Furthermore, the success experience...Show moreLast updated: 30+ days ago
Product Manager

Product Manager

PelicanLaval, Quebec
CA$53.85 hourly
The Product Manager is responsible for carrying out marketing research, managing and executing nautical product plans focused on consumer segments and mass retailer needs. He / she must build personas...Show moreLast updated: 30+ days ago
Senior CRA / Clinical Research Associate- FSP

Senior CRA / Clinical Research Associate- FSP

ParexelRemote, Quebec, Canada
30+ days ago
Job type
  • Remote
Job description

When our values align, there's no limit to what we can achieve.

Parexel FSP is looking for a CRA in the Ontario and Quebec Area of Canada.

Cell Therapy Trial experience strongly preferred.

Job Purpose :

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team / Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.

The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

Key Accountabilities :

Site Management Responsibilities

  • Contributes to the selection of potential investigators.
  • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application / documents to EC / IRB and to Regulatory Authorities for start-up and for the duration of the study.
  • Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
  • Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
  • Actively participates in Local Study Team (LST) meetings.
  • Contributes to National Investigators meetings, as applicable.
  • Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality / performance) within the LST.
  • Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
  • Updates CTMS and other systems with data from study sites as per required timelines.
  • Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
  • Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines, and discusses with LSAD the correct timing and type of visits.
  • Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
  • Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
  • Ensures data query resolution in a timely manner.
  • Works with data management to ensure robust quality of the collected study data.
  • Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
  • Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
  • Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
  • Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and / or Clinical Quality Management (CQM) as required.
  • Assists site in maintaining inspection ready ISF.
  • Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
  • Ensures timely collection / uploading of essential documents into the eTMF in accordance with ICH-GCP, Client SOPs and local requirements. Supports / participates in regular QC checks performed by LSAD or delegate.
  • Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
  • Provides feedback on any research related information including sites / investigators / competing studies that might be useful for the local market.
  • Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line manager.

Compliance with Sponsor Standards

  • Ensures compliance with the Client’s Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).
  • Ensures compliance with local, national, and regional legislation, as applicable.
  • Completes timesheets accurately as required.
  • Compliance with Parexel Standards

  • Complies with required training curriculum.
  • Completes timesheets accurately as required.
  • Submits expense reports as required.
  • Updates CV as required.
  • Maintains working knowledge of and complies with Parexel / Client processes, ICH-GCPs and other applicable requirements.
  • Skills (Essential) :

  • Excellent attention to detail.
  • Good written and verbal communication skills.
  • Good collaboration and interpersonal skills.
  • Good negotiation skills.
  • Proficient in written and spoken English language required.
  • Fluency in local language(s) required.
  • Skills (Desirable) :

  • Ability to work in an environment of remote collaborators.
  • Manages change with a positive approach for self, team, and the business. Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods / processes of delivering quality clinical trials with reduced budget and in less time.
  • Good analytical and problem-solving skills.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems / software in an e-enabled environment.
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
  • Knowledge and Experience (Essential) :

  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP / GDP.
  • Good knowledge of relevant local regulations.
  • Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
  • Basic understanding of the drug development process.
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
  • Knowledge and Experience (Desired) :

  • Familiar with risk-based monitoring approach including remote monitoring.
  • Good cultural awareness.
  • Education :

  • Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification (adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
  • Other :

  • Ability to travel nationally / internationally as Required
  • Valid driving license per country requirements, as applicable.