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Research nurse Jobs in Granby, QC

Last updated: 2 days 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
nurse

nurse

CIUSSS de l'Estrie-CHUSGranby, QC, CA
CA$27.08–CA$47.98 hourly
Permanent
Address and document symptoms and changes in patients' conditions.Assess patients to identify appropriate nursing interventions. Collaborate with members of an interdisciplinary health team to plan,...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
Registered Nurse (RN) - Rigaud

Registered Nurse (RN) - Rigaud

RhynoCareRigaud, Ontario, Canada
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
  • Promoted
Administrative Assistant Admin Work At Home - Part-Time Online Focus Group Panel

Administrative Assistant Admin Work At Home - Part-Time Online Focus Group Panel

ApexFocusGroupSaint-Félix-d'Otis, Quebec, Canada
CA$750.00 weekly
Remote
Full-time +2
We're now accepting participants for focus group studies! You can earn up to $750 per week working part-time from home.Simply register to see if you qualify—no experience as an administrative assis...Show moreLast updated: 2 days 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
  • Promoted
DevOps Engineer - Renewable 6-month contract

DevOps Engineer - Renewable 6-month contract

freelance.caGranby, Canada
Temporary
If you are looking to advance your career and seek a new stimulating challenge, join our dynamic and innovative team.Do you want to advance your career? Need a new challenge?.Our client is looking ...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
UX Writer

UX Writer

Bentley SystemsHome or Hybrid, QC, CA
Office-Based Burlington, Ontario / Home-Based Canada .We are seeking an experienced and creative UX Writer to join our global Digital Design team. In this role, you will be responsible for crafting...Show moreLast updated: 30+ days ago
statistical technician

statistical technician

Groupe Biscuits LeclercQC, CA
CA$68,560.00 yearly
Permanent
Heures de travail : 40 hours per week.Logistics, materials, and supply chain management.Private company, corporation or industry. Collect, consolidate, cross-tabulate and format data.Compile tables, ...Show moreLast updated: 5 days ago
Buyer

Buyer

St-AmourLaurentians
CA$100,000.00–CA$120,000.00 yearly
Permanent
Located on the North Shore of Montreal, more precisely in Terrebonne.This company specializes in electrical disconnect switches and plays a crucial role in Canada's energy sector.Highly reliable, c...Show moreLast updated: 30+ days ago
Registered Nurse

Registered Nurse

Bayshore HealthCareNorthern Quebec - Remote regions, Quebec, Canada
Remote
Full-time +2
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...Show moreLast updated: 16 days ago
  • Promoted
Work from Home Product Testing $25-$45 per hour

Work from Home Product Testing $25-$45 per hour

OCPAQuebec, 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
systems designer - hardware

systems designer - hardware

SII CanadaQC, CA
CA$80,000.00–CA$95,000.00 yearly
Permanent
Lead and co-ordinate teams of design professionals in the development and integration of information and communication system architecture, hardware and software. Research, evaluate and integrate ne...Show moreLast updated: 3 days ago
  • Promoted
Remote Part Time Data Entry Work From Home Computer Job

Remote Part Time Data Entry Work From Home Computer Job

EA SolutionsGranby, QC, ca
CA$34.00 hourly
Remote
Full-time +1
Remote Part Time Data Entry Work From Home Computer Job.Work from Home Administration - Computer Online Data Entry & Short Studies / Feedback - Part Time & Full Time Work - No Experience Need...Show moreLast updated: 30+ days ago
Senior Technical Designer - Menswear and Mens and Womens Outerwear

Senior Technical Designer - Menswear and Mens and Womens Outerwear

Proforce PersonnelQuebec, CA
Full-time +1
Thank you in advance, but please do not apply to this position if you do not have a valid work permit • •.Our client, a manufacturer of Mens and Womens cutting edge fashion trends, is looking for an ...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.