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1–2 jobs· newest first

Data CoordinatorNew
McKesson · Denver, US
$23–$27
Research Coordinator - Kidney Health
University of Alberta · Edmonton, Canada
On-site · Contract · Manager

+10K new in the last hour

Data Coordinator

McKesson · Posted Nov 9, 2026

Denver, Colorado, United States
$23–$27 per hour

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Supports Study Coordinators in clinical trial data management and regulatory compliance.

Compensation

Pay range $23/hr - $27/hr

Responsibilities

Supports Study Coordinators to meet industry trial data deadlines
Obtains source documentation for patients enrolled into clinical trial
Assists Study Coordinators with case report form completion and query resolution
Assists in Serious Adverse Event (SAE) reporting and tracking
Creates and maintains patient visit tracking spreadsheets for Study Coordinators

Requirements

Bachelor's degree
Nice to have: Healthcare experience
Nice to have: Clinical trials support
Nice to have: Pharmaceutical industry experience

Skills

Knowledge of GCP Knowledge of GMP Source documentation Case report form completion Serious Adverse Event reporting Spreadsheet management Excel

Benefits

Total Rewards package
Comprehensive benefits

See full job description

Research Coordinator - Kidney Health

University of Alberta · Posted Nov 6, 2026

Edmonton, Alberta, Canada
On-site
Contract · Manager
5+ years

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Coordinate and supervise clinical research studies within the Kidney Health Research Group at the University of Alberta.

Responsibilities

Coordinate and supervise multiple clinical research studies
Develop, execute, and evaluate clinical research protocols
Manage study logistics and compliance
Prepare and submit ethics and regulatory documents
Maintain study documentation and data management

Requirements

Bachelor's degree required
RN, BScN active designation, Masters or PhD in relevant fields are assets
Nice to have: Certified Clinical Research Professional (CCRP) designation
Nice to have: SPOR Pragmatic Clinical Trials certificate
Nice to have: Nephrology related care experience

Skills

Clinical research coordination Good Clinical Practice Regulatory compliance Data management Case report form completion Ethics submissions

Project management

Problem solving

Electronic clinical information systems

Clinical trial data management platforms

Benefits

Comprehensive benefits package

See full job description