Research Coordinator at Hamilton Health Sciences Corporation

Hamilton, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

06 Jul, 26

Salary

0.0

Posted On

07 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical trial management, Regulatory compliance, Study activation, Data collection, Project management, Medical terminology, Time management, Critical thinking, Relationship building, Problem solving, Microsoft Office, Ethics submissions, ICH-GCP guidelines, Vendor software management, Clinical research principles

Industry

Hospitals and Health Care

Description

Reporting to the Clinical Manager, the Research Coordinator’s purpose is to facilitate the activation of new studies and the coordination and management of moderately complex interventional clinical trials from activation to closeout adhering to regulatory requirements and the study protocol. The Research Coordinator is responsible for performing study-specific duties delegated by Principal Investigator (PI), and must utilize good organizational, time management, and critical thinking skills to efficiently activate clinical trials and independently coordinate assigned studies, solve problems, and manage multiple priorities at the same time. •Undergraduate Degree in Sciences or Health Sciences • Clinical research certification required, i.e., ACRP, SoCRA or post-graduate certifi cation in clinical research • Minimum 3 years previous experience in clinical trials; oncology clinical trials preferred • Experience using clinical trial data management, ethics submission, and vendor software applications, and sponsor portals • Previous experience with ethics submissions and completion of regulatory documents • Fundamental knowledge of clinical research principles, practices, and processes related to study coordination, data collection, and reporting • Applies thorough knowledge of clinical research principles, practices, and processes to facilitate study activation • Utilizes relationship-building skills to cultivate effective partnerships with study sponsors and internal and external collaborators • Excellent communication and problem-solving skills • Working knowledge of project management processes • Working knowledge of ICH-GCP Guidelines and international research regulations • Knowledge of medical terminology required • Excellent organizational and time management skills • Excellent computer skills including extensive experience with Microsoft Office applications

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Responsibilities

The Research Coordinator facilitates the activation and management of interventional clinical trials from start to finish while adhering to regulatory requirements. They perform delegated study-specific duties and collaborate with internal and external partners to ensure efficient trial execution.