Winnipeg Mb Clinical research associate Jobs – 5 Openings This Week

Clinical Research Associate - Contract
Clinical Development Solutions —Winnipeg, MB
- Contract
- Remote
- Microsoft Excel
- Microsoft Outlook
- Bachelor's
Quick apply
11d
CANADA RESEARCH CHAIR TIER 1
University of Manitoba —Winnipeg, MB
- Doctoral degree
- Research
- Bachelor's
Chef de projet associé, Mesure (Measurement Associate Project Manager), IQVIA Digital
IQVIA —Winnipeg, MB
- $70,500–$117,500 a year
- Full-time
- Customer service
- Bachelor's
- Computer skills
Assistant, Associate, or Professor - Internal Medicine
University of Manitoba —Winnipeg, MB
- Full-time
- Medicine
- Doctoral degree
- Research
Tier 2 Canada Research Chair - Immunology
University of Manitoba —Winnipeg, MB
- Full-time
- Doctoral degree
- Research
- Bachelor's

More jobs to discover

Find similar jobs that you might be interested in.

CANADA RESEARCH CHAIR TIER 1
University of Manitoba —Winnipeg, MB
The University of Manitoba is committed to the principles of equity, diversity & inclusion and to promoting opportunities in hiring, promotion and tenure (where…
Tier 2 Canada Research Chair - Immunology
University of Manitoba —Winnipeg, MB
Applicants who are more than 10 years from having earned their highest degree (and where career breaks exist, such as maternity or parental leave, extended sick…

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Clinical Safety Data Associate
Everest Clinical Research —Markham, ON
To drive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning…
$60,000–$80,000 a year
Quick apply
Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2026-18011
Sunnybrook Health Sciences Centre —Toronto, ON
Sunnybrook Health Sciences Centre is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to…
Quick apply

Show more jobs in cities nearby

I want to receive the latest job alerts for clinical research associate in winnipeg mb

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical research associate jobs near winnipeg mb

Clinical Research Associate jobs in Winnipeg, MB

Chairperson jobs in Winnipeg, MB

Dental Associate jobs in Vancouver, BC

Clinical Research Associate jobs in Vancouver, BC

Associate Professor jobs in Port Perry, ON

Store Associate, Dollarama jobs in Moncton, NB

Associate Professor jobs in Edmonton, AB

Associate Professor jobs in Toronto, ON

Clinical Data Analyst jobs in Toronto, ON

Clinical Research Associate jobs in Montréal, QC

Research Assistant jobs in Hamilton, ON

Clinical Research Associate jobs in Ville De Québec, QC

Clinical Research Associate jobs in Remote

Policy Research jobs in Toronto, ON

Chef De Projet jobs in Brossard, QC

Ciusss Du Centre Ouest De L'île De jobs in Montréal, QC

Chef De Projet jobs in Montréal, QC

Remote Chef, Oil Rigs jobs in British Columbia

Chef De Projet jobs in Toronto, ON

Chef De Projet jobs in Remote

Clinical Research Associate - Contract

Clinical Development Solutions
Winnipeg, MB

Quick apply

Job details

Contract
11 days ago

Qualifications

Data quality auditing
Computer operation
Microsoft Excel
Microsoft Outlook
Clinical research
Case file maintenance
Bachelor's
Data management
Report and presentation preparation
Quality Control
Written report writing
Recruiting
Clinical trials
Data validation
Status Reporting
Standard operating procedures (SOPs)
Communication skills
Project progress tracking

Full job description

Job Summary:

CDS is looking for a local (Winnipeg Based) Clinical Research Associate (CRA) to perform the clinical monitoring aspects for specific projects on a contract basis.

The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing selection, initiation, periodic monitoring and close-out of investigational sites in accordance with ICH GCP guidelines.

Duties and Responsibilities:

May conduct pre-study site assessment/qualification visits, collection and review essential documents, prepare evaluative reports; participate in the final selection of investigators and study sites and participate in study start-up activities.
May conduct site initiation visits; advise and train site personnel on sponsor and regulatory requirements for study; participate in site meetings and multi-centre investigator meetings and prepare visit reports.
Site Management Activities, including maintain all essential clinical documents and manage supply of investigational product throughout the trials
Conduct site monitoring visits and follow-up on any outstanding issues; ensure all clinical aspects of the studies are being carried out in accordance with the clinical protocol, ICH GCP, state/provincial and federal/country regulations, guidelines and policies; and prepare site status reports and monitoring visit reports.
Review site files and records, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identify deficiencies and discrepancies; and provide remedial training and/or initiate corrective action as required.
May conduct investigator site close-out visits and assist in the termination of clinical studies by identifying items and issues for review and/or follow-up; collection of necessary documents, reconciliation of study drug/device and disposition, review of completeness and accuracy of files, retrieval of relevant codes, prepare study close-out / termination reports.
Assist in the reconciliation of and follow up on adverse event reporting, and serious adverse event reporting to ensure appropriate notification and compliance with regulatory agency, IRB/REB and SOPs
May assist sites with preparation for regulatory agency, sponsor, or IRB/REB audits.
Current projects are local (Winnipeg). Future projects may involve travel within Canada & USA up to 60%.
May perform other miscellaneous job-related duties as assigned.

Interacts with (where applicable):

Sponsor personnel. This may include Lead CRA, Project Management, Documentation Personnel, Trial Assistants, Data Management & Clinical Safety.
Internal Quality Assurance.
Associated or trial related Contract Research Organizations (CROs).
Internal Lead CRA, Project Management, Documentation Personnel, Trial Assistants, & Clinical Safety.
Investigational Site Personnel (Principal Investigator, Research Coordinator, etc.).
Clinical Team (other monitors, etc).

Competencies:

Must possess excellent written and verbal communication skills and have the ability to develop and deliver both oral and written presentations.
Ability to make evaluative judgments.
Ability to provide advice, guidance, and support to professional staff in area of specialty
Ability to develop and implement clinical research monitoring plans and standard operating procedures.
Ability to communicate and interact competently and professionally at all levels within a broad, complex clinical research environment.

Qualifications:

Bachelor's degree in life sciences or related field or certification in a related allied health profession from an appropriately accredited institution (i.e. BN, RN, MT, PA, RPh, RT) GCP Certification, or certification with SoCRA or ACRP preferred.
A minimum of 2 years experience in clinical research or related research field preferred.
Knowledge of all regulations and guidelines pertaining to the conduct of clinical trials on human subjects (i.e. ICH GCP, FDA and Health Canada regulations).
Knowledge of randomized controlled clinical trials principles, methodology, and procedures.
Knowledge of current and developing trends and standards in clinical trials monitoring.
Computer/Laptop usage skills (knowledge of Microsoft Office, including Word, PowerPoint, Excel and Outlook).

Accountability:

Ensures compliance with all regulatory and contractual requirements by quality controlling the execution of clinical protocol and data management for a clinical trial(s) at multiple sites.
Ensures validity of studies by establishing and maintaining sound clinical and data collection practices.
Ensures compliance with established protocols, regulatory and contractual requirements; appropriate research methodology; and study timelines by monitoring the conduct and progress of the studies.
Ensures appropriate transmission of clinical case data to the data management centre(s); reviews case report queries and problems, and assists in data review and correction as appropriate.

Application question(s):

This position does not require you to come in to the office located in Winnipeg, MB. However you must live close to the office. Do you live in or around Winnipeg, MB?

Work Location: Remote

Quick apply

Refine Your Search

clinical research associate jobs in winnipeg mb

Clinical Research Associate - Contract

CANADA RESEARCH CHAIR TIER 1

Chef de projet associé, Mesure (Measurement Associate Project Manager), IQVIA Digital

Assistant, Associate, or Professor - Internal Medicine

Tier 2 Canada Research Chair - Immunology

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alerts for clinical research associate in winnipeg mb

Explore jobs in more locations

Job seeker tools

Employer Tools

Browse

Stay Connected