Hybrid Senior Clinical Research Associate — Trials Leader

Placements24; Noord-Kaap; Hybrid; CAD 56,000 - 77,000; Full time

Benefits offered by this job

Health insurance

Retirement annuity

Bonuses

Professional development

Job summary

Placements24 in Kimberley, SA, seeks an experienced Senior Clinical Research Associate to oversee trials at investigator sites, ensure protocol and GCP compliance, and maintain trial data integrity in a hybrid role with on-site visits and remote tasks.

You will monitor sites, verify data, manage recruitment, and train site personnel while collaborating with sponsors and study teams to drive trial progress.

Qualifications

• 4+ years of experience as a Clinical Research Associate or similar role.
• Thorough understanding of ICH-GCP and regulatory requirements.
• Proven site monitoring and documentation experience.
• Strong communication and organizational skills; travel to sites required.

Responsibilities

• Conduct site initiation, monitoring and close-out visits per SOPs.
• Verify data against source documents and CRFs for quality control.
• Manage subject recruitment and retention at investigator sites.
• Ensure regulatory compliance and study protocol adherence.
• Build relationships with investigators and site staff.
• Oversee investigational product accountability and dispensing records.
• Provide training to site personnel on study procedures.
• Prepare monitoring visit reports promptly.
• Raise issues and risks to CTM and stakeholders as needed.
• Participate in study team meetings to support trial success.

Skills

Communication skills

Organization

Problem-solving

Travel readiness

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related healthcare field

Tools

CTMS

EDC systems

Job description

Placements24 in Kimberley, SA, seeks an experienced Senior Clinical Research Associate to oversee trials at investigator sites, ensure protocol and GCP compliance, and maintain trial data integrity in a hybrid role with on-site visits and remote tasks.

You will monitor sites, verify data, manage recruitment, and train site personnel while collaborating with sponsors and study teams to drive trial progress.