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Clinical research associate Jobs in Toronto, ON

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Clinical research associate • toronto on

Last updated: 15 hours ago

Clinical Research Associate

Macpower Digital Assets Edge Private LimitedToronto, ON
Full-time +1

Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols.Ensures coordinati... Show more

Consumer Research Associate (Remote)

GL IncWillowdale, Ontario
CA$15.00 hourly
Remote
Part-time +1

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 more

 • Promoted

Study Coordinator - Clinical Research

Pharma Medica Research Inc.Toronto, Ontario, Canada
CA$50,000.00 yearly
Full-time

Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trails in healthy volunteers, special and patient populations.We are currently... Show more

Research Coordinator

Randstad CanadaNorth York, Ontario, CA
Temporary
Quick Apply

As a Research Coordinator, you will assist the department with basic day-to-day administrative duties.The details of this role that will help you decide if it’s the right move for you….Assignment D... Show more

Senior Research Specialist, Product Development and Research

Royal Bank of Canada>TORONTO, Canada
CA$90,000.00–CA$140,000.00 yearly
Full-time

RBC Global Asset Management (RBC GAM) is the asset management division of Royal Bank of Canada (RBC) and includes leading money managers such as BlueBay Asset Management and Phillips, Hager & North... Show more

Research Manager

hireVouchToronto, Ontario, USA
Full-time

You will be part of  a group dedicated to supporting external clients with consumer insights and industry benchmarks on North American wealth management.You will manage the operation, analysis, del... Show more

Clinical Nurse Educator

Spectrum Health CareToronto, Ontario, Canada
CA$85,000.00–CA$95,000.00 yearly
Full-time

Plans, delivers, and evaluates competency-based orientation and continuing education programs.Conducts needs assessments, provides recommendations, and plans and implements education programs with ... Show more

Market Research Associate - No Experience

Clubshop | USToronto, Ontario
Full-time

Discover The System Surveoo That’s Helping Newbies Earn Daily.Turn your free time into daily earnings by answering simple surveys.No product or tech skills needed.Join For Free And Start Earn... Show more

Market Research & Data Associate (Remote)

ProprofitworldToronto, ON, Canada
Remote
Part-time
Quick Apply

Proprofit Worldwide Ltd is expanding its remote digital research division.We are currently looking for independent Market Research Assistants to support our digital market research and data coordin... Show more

 • New!

Clinical Manager

Child Development InstituteToronto, ON, CA
CA$94,000.00–CA$111,000.00 yearly
Full-time
Quick Apply

Who we are Our mission is to transform the lives of children, youth and their families by developing and delivering innovative, research-based mental health and early learning programs.Child Develo... Show more

Clinical Research Coordinator

Centricity ResearchToronto, Ontario, Canada, M4G 3E8
CA$55,000.00–CA$62,500.00 yearly
Full-time +1
Quick Apply

Join Us at Centricity Research!.Centricity Research is one of the largest clinical research networks in North America.We are a fully centralized Integrated Research Organization (IRO) specializing ... Show more

Clinical Assistant

WELL Health Technologies CorpToronto, Ontario, Canada, M9N 1X2
CA$18.00–CA$20.00 hourly
Part-time
Quick Apply

WELL Health Clinic Network Inc.WELL Health - Weston & Lawrence, Toronto, ON.WELL Health Technologies is an innovative technology-enabled healthcare company whose overarching objective is to positiv... Show more

Senior Research Coordinator

BaycrestToronto, CA
CA$66,021.00 yearly
Full-time

The Rotman Research Institute at Baycrest.The Anne and Allan Bank Centre for Clinical Research Trials in the Rotman Research Institute of the Academy for Research and Education at Baycrest Centre f... Show more

Research Analyst - Gracorp

GrahamToronto, ON, CA
Full-time

At Gracorp, the development arm of the Graham Group, we create places that redefine communities and deliver lasting value.As part of our agile and entrepreneurial team, you’ll contribute to transfo... Show more

Allergist / Clinical Immunologist

Foundation Health CanadaEtobicoke, Ontario, Canada
Full-time

Foundation Health is a patient-centered, multidisciplinary healthcare organization committed to delivering high-quality, accessible care across Ontario.Our integrated care model connects primary ca... Show more

Clinical Research Coordinator

University of TorontoToronto, ON, CA
Full-time

Department of Pharmacology and Toxicology.Home to over 40 departments and institutes, the University of Toronto's Temerty Faculty of Medicine lies at the heart of the Toronto Academic Health Scienc... Show more

Clinical Trial Manager, Clinical Operations, Infectious Disease

ModernaToronto, Canada
Full-time

Joining Moderna means advancing mRNA science to transform medicine.Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is str... Show more

Clinical Counsellor

Workplace OptionsToronto, ON, CA
Full-time
Quick Apply

Who we are: At Workplace Options (WPO), we deliver human-centric solutions that empower people to thrive - personally and professionally.With a global team of more than 4,800 professionals, we prov... Show more

AI Research Engineer

DeloitteToronto, ON, ON, CA
Permanent

Toronto, ON; Brossard, QC; Burlington, ON; Calgary, AB; Edmonton, AB; Fredericton, NB; Halifax, NS; Kitchener, ON; Laval, QC; Moncton, NB; Montreal, QC; Ottawa, ON; Quebec City, QC; Regina, SK; Sai... Show more

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Clinical Research Associate

Clinical Research Associate

Macpower Digital Assets Edge Private LimitedToronto, ON
30+ days ago
Job type
  • Full-time
  • Temporary
Job description

Job Summary:

  • Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols.
  • Ensures coordination of interim and closeout activities associated with clinical trials to ensure timelines and metrics are met and maintained throughout the study. This is a contract traveling CRA position if necessary.

Responsibilities:

  • Has a solid knowledge of the therapeutic area or a therapeutic background, showing adeptness to work in oncology and phase 1 studies.
  • Performs regulatory document review and monitors adherence to the regulatory document collection process.
  • Able to write clinical monitoring plans, source documents, and create other study tools when requested.
  • Conducts monitoring/co-monitoring activities for interim site monitoring and closeout visits, in conformance with all relevant laws, regulations, guidelines, protocols, and internal SOPs/policies.
  • Identifies and effectively documents site findings with the ability to re-train, place corrective action in place with the site, and follow up as required.
  • Verifies study documents (e.g., case report forms, source documents, adverse events) are tracked and reviewed for completeness and accuracy to ensure data integrity.
  • Reconciles clinical supplies and drug accountability records at study sites.
  • Identifies and effectively documents site findings with the ability to re-train, place corrective action in place with the site, and follow up as required.
  • Reviews, clarifies, and obtains data changes via query resolutions with site personnel.
  • Collaborates with data management to resolve queries.
  • Prepares telephone contact reports, confirmation letters, site visit reports (PSV, SIV, IMV, and COV), and follow-up letters to accurately and completely document site status and activities.
  • Understands and implements processes for distribution and tracking of SAEs, safety documentation, and pregnancies.
  • Monitors compliance with these processes.
  • Facilitates investigator site payments, as applicable.
  • Reviews/creates/tracks trial newsletters, memos, mass correspondence, or other appropriate trial-related documentation.
  • Obtains a complete understanding of all trial-related documents and operational procedures.
  • Maintains clinical trial tracking information pertaining to the study (e.g., monitoring calendar, monitoring reports, phone contacts).
  • Assists with auditing of study files and retrieval of outstanding documents as needed (in-house and on-site document reconciliation).
  • Reviews and tracks study documents, including project files both electronically and in the Trial Master File and Project Status Reports.
  • Communicates and interacts with relevant study personnel, including developing and maintaining collaborative relationships to manage study issues and support milestone achievement; conveys project information; answers study questions in a timely manner while using discretion when to escalate to the study manager; troubleshoots and follows up on study progress; and reviews report data for completeness and accuracy.
  • Assists with effective and timely audit/inspection responses.
  • Prepares key reports and documents on the progress of the study for the study manager.
  • Tracks study-specific tasks and progress of the trial.
  • Reviews study and/or site-specific ICF(s) for compliance with ICH/GCP and company SOPs.