Clinical Research Coordinator

Placements24; Kimberley; Hybrid; CAD 60,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Retirement plan

Paid time off

Job summary

Placements24 is seeking a dedicated Clinical Research Coordinator to join their team in Kimberley, Canada, in a hybrid role. You will manage participant recruitment, data collection, and follow-up while ensuring protocol compliance and regulatory standards.

You will work with investigators, sponsors, and regulatory bodies to ensure efficient trial operations and ethical conduct. Strong organizational and communication skills are essential in a fast-paced environment.

Qualifications

• Bachelor's degree in a life science, nursing, or related field.
• Master's degree preferred.

Responsibilities

• Recruit, screen, and enroll eligible participants according to protocol.
• Collect, manage, and maintain accurate study data with confidentiality.
• Schedule and coordinate study visits, assessments, procedures, and sample collection.
• Educate participants about procedures, risks, and benefits and obtain informed consent.
• Monitor adverse events and report according to regulatory guidelines.
• Liaise with investigators, sponsors, regulators, and stakeholders to ensure smooth operations.

Skills

Organizational skills

Communication

Prioritization

Education

Bachelor's degree in life science / nursing

Master's degree preferred

Tools

EDC systems

Clinical trial management software

Job description

About the Role

Our client is seeking a dedicated and organized Clinical Research Coordinator to join their team in Kimberley . This hybrid role plays a vital part in the successful execution of clinical trials, ensuring compliance with protocols and regulatory standards. You will be responsible for managing patient recruitment, data collection, and participant follow-up, working closely with investigators, study sponsors, and regulatory bodies. This position requires strong organizational skills, attention to detail, and a commitment to advancing medical research through ethical and efficient trial management.

Key Responsibilities

• Recruit, screen, and enroll eligible participants for clinical trials according to protocol requirements.
• Collect, manage, and maintain accurate and complete study data, ensuring data integrity and confidentiality.
• Schedule and coordinate study visits, including assessments, procedures, and sample collection.
• Educate participants about study procedures, risks, and benefits, ensuring informed consent is obtained and maintained.
• Monitor participants for adverse events and report them promptly according to regulatory guidelines.
• Liaise with investigators, study sponsors, regulatory agencies, and other stakeholders to ensure smooth trial operations.

Requirements

• Bachelor's degree in a life science, nursing, or related field; Master's degree preferred.
• Minimum of 3 years of experience as a Clinical Research Coordinator or similar role.
• Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, ICH).
• Experience with electronic data capture (EDC) systems and clinical trial management software.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple priorities and work effectively in a hybrid setting.

Benefits

• Competitive salary and potential for annual bonuses.
• Comprehensive health, dental, and vision insurance coverage.
• Retirement plan options.
• Generous paid time off and holidays.
• Opportunity to contribute to life‑saving medical advancements.