Clinical Research Associate (Remote)

Placements24; Stellenbosch; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Laptop & phone

Home office stipend

Health insurance

Paid time off

Professional development

Job summary

Placements24 is seeking an experienced Clinical Research Associate to join our global operations team. This fully remote role will support clinical trials from anywhere in South Africa, with responsibilities across site selection, initiation, monitoring, and close-out to ensure data integrity and patient safety.

Ideal candidates hold a life science degree and 3–5 years CRA experience, with strong knowledge of GCP/ICH guidelines and proficiency in CTMS/EDC tools.

Qualifications

• Experience with GCP and ICH guidelines in clinical trials.
• Bachelor’s degree in life sciences or related field; advanced degree preferred.
• Ability to manage multiple sites and complex protocols independently.

Responsibilities

• Conduct site visits (selection, initiation, monitoring, close-out) per protocol and SOPs.
• Ensure regulatory compliance with GCP, ICH and local rules.
• Verify data integrity via source data verification.
• Train site staff on protocol requirements and data collection.
• Serve as primary contact for assigned sites; escalate issues as needed.
• Prepare monitoring reports and communicate findings to management.

Skills

GCP knowledge

ICH guidelines

Communication

Organizational skills

Education

Bachelor's in life science

Advanced degree a plus

Tools

CTMS

EDC

Job description

About the Role

Our client is seeking an experienced and independent Clinical Research Associate (CRA) to join their global clinical operations team, working remotely from anywhere within South Africa . This role is essential for managing and monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring data integrity and patient safety. This is an excellent opportunity for a seasoned CRA looking for a fully remote position with a respected pharmaceutical organization committed to advancing healthcare through rigorous clinical research.

Key Responsibilities

• Conduct site visits (selection, initiation, interim monitoring, and close-out) as required by the clinical trial protocol and company SOPs.
• Ensure compliance with all regulatory requirements, including GCP, ICH guidelines, and local regulations.
• Verify the accuracy, completeness, and integrity of clinical data through source data verification.
• Train and support study site staff on protocol requirements, study procedures, and data collection.
• Act as the primary point of contact for assigned clinical trial sites, fostering strong working relationships.
• Identify, resolve, or elevate site-level issues and deviations promptly.
• Prepare monitoring reports and communicate findings and action plans to study management.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree is a plus.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry.
• Demonstrated knowledge of GCP, ICH guidelines, and clinical trial conduct.
• Proven ability to manage multiple clinical trial sites and complex protocols independently.
• Excellent communication, interpersonal, and organizational skills.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.

Benefits

• Competitive remote salary and performance-based incentives.
• Comprehensive health, dental, and vision insurance.
• Company-provided laptop and mobile phone, with a home office stipend.
• Generous paid time off and opportunities for professional development.
• Flexible work schedule and the autonomy to manage your own workload.