Talent.com

Clinical data associate Jobs in Old toronto, ON

Create a job alert for this search

Clinical data associate • old toronto on

Last updated: 1 day 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

Associate Director - Data & AI Solutions Architect

0000050007 Royal Bank of CanadaTORONTO, Ontario, Canada
Full-time

Capital Markets Quantitative & Technology Services - Data AI and Research Technology (DART) team is looking to hire a Data & AI Solution Architect to design secure, scalable and cost-effective data... Show more

Senior Associate, Market Data Services

Royal Bank of Canada>TORONTO, Canada
Full-time

The global Market Data Services team consists of three sub-groups (MDS Administration, MDS Solutions and MDS Compliance) who engage, strategize and support enterprise-wide businesses and stakeholde... Show more

Data Architect / Data Modeler

Astra North Infoteck Inc.Toronto, ON, ca
Full-time

Data Architect / Data Modeler – Azure, AWS, Data Warehousing & Informatica CDI.Hybrid (2 days per week in-person at Toronto office preferred).Informatica CDI (Cloud Data Integration).Data Archi... Show more

Associate Director, Data Center Management

1110 Kyndryl Canada LimitedToronto HQ
Full-time

At Kyndryl, we run and reimagine the mission-critical technology systems that drive advantage for the world’s leading businesses.We are at the heart of progress; with proven expertise and a continu... Show more

Account Manager, Clinical Diagnostic

RenaudExecToronto
CA$52.20 hourly
Permanent

Our client, a leader in manufacturing capital equipment for the hospital environment is looking for an Account Manager based in GTA to cover the Ontario region.The account manager will be responsib... Show more

Senior Associate - Market Data Services

Randstad CanadaToronto, Ontario, CA
Permanent
Quick Apply

On behalf of our client, a leading global financial institution, we are seeking a highly skilled Senior Associate, Market Data Services (MDS) Compliance.In this role, you will join a high-performin... Show more

Clinical Product Specialist

Clarius Mobile HealthToronto, Ontario, CA
Full-time

Today, as many as 25 million medical professionals globally don't have access to medical imaging, which is proven to improve patient care and reduce healthcare costs.That's why we're on a mission t... Show more

Senior Clinical Research Asssociate

AbbVieToronto, Ontario, Canada
Remote
Full-time

Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance.... Show more

Data Scientist/Data Engineer

hireVouchToronto, Ontario, USA
Full-time

Data Scientist (AI & Data Engineering) – External Data & Intelligent Insights.Our client is a global real estate investor, developer, and manager connects people to exceptional places across the of... Show more

Manager, Clinical Data Management

Everest Clinical Research Services IncToronto, Ontario
CA$140,000.00 yearly
Full-time

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biote... Show more

Associate Director, Business Data Office, Data Integrity & Operations

MUFG Investor ServicesToronto, Ontario, Canada
Full-time

You will be responsible for ensuring the operational integrity and continuous improvement of core business data domains.The role combines ownership of daily data operations, including MDM data supp... 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

Senior Clinical Research Associate

PSI CROToronto, Ontario, Canada
Remote
Full-time

We are looking for an experienced freelance Sr.CRA to support us with the following responsibilities in Canada:.Conduct and report SIV, RMV, COV onsite monitoring visits.Perform CRF ... Show more

Associate Director, Data Centres

Turner & TownsendToronto, Canada, CA
CA$135.00 daily
Full-time

Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries.Working with our clients across real estate, infrastructure, energy and natural resourc... Show more

Clinical Implementation Specialist

Able InnovationsToronto, ON, CAN
CA$60,000.00 yearly
Full-time
Quick Apply

Clinical Implementation - Toronto, ON (IST2608)Passionate about healthcare innovation and adoption? Do you love working with people and making complex things feel approachable?Become a healthcare t... Show more

Clinical Associate (French Speaking)

ICONToronto
Permanent

Clinical Associate - Hybrid Role - French Speaking - Toronto, Canada.ICON plc is a world-leading healthcare intelligence and clinical research organization.We’re proud to foster an inclusive envir... Show more

Associate Professor - Clinical and Counselling Psychology

University of TorontoToronto, ON, CA
Full-time +1

Faculty - Tenure Stream (continuing).Ontario Institute for Studies in Education.Department of Applied Psychology and Human Development.The Department of Applied Psychology and Human Development (AP... 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

People also ask
Clinical Research Associate

Clinical Research Associate

Macpower Digital Assets Edge Private LimitedToronto, ON
9 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.