Remote Clinical Research Associate for Global Trials

Placements24; Benoni; Hybrid; ZAR 420,000 - 630,000; Full time

Benefits offered by this job

Fully remote work arrangement

Professional development support

Competitive salary with incentives

Job summary

Placements24 is seeking a skilled Pharmaceutical Clinical Research Associate (CRA) to join a globally integrated, fully remote team with operations extending to the Benoni area. This role monitors study sites, ensures data integrity, and protects patient safety throughout the trial lifecycle.

The ideal candidate has a Bachelor's degree in life sciences and at least 3 years of CRA experience, with strong knowledge of GCP/ICH and regulatory requirements.

Qualifications

• Bachelor's degree in life sciences or related field.
• Minimum 3 years of CRA experience in the pharmaceutical industry.
• Thorough understanding of GCP, ICH, and regulatory requirements.
• Experience with EDC and CTMS.
• Willingness to travel and work independently in a fully remote capacity.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocol, GCP, and regulatory requirements.
• Perform site initiation, routine monitoring, and close-out visits for assigned sites.
• Verify accuracy, completeness, and integrity of trial data through source data verification.
• Ensure patient safety by monitoring adverse events and reporting per protocol and regulations.
• Build and maintain relationships with investigators, site staff, and participants.
• Provide training and ongoing support to trial sites on procedures and data collection.

Skills

GCP/ICH knowledge

Site monitoring

Regulatory compliance

Data integrity

EDC systems

CTMS proficiency

Remote work capable

Excellent communication

Travel flexibility

Education

Bachelor's degree in life sciences

Master's degree (a plus)

Tools

CTMS

EDC software

Job description

Placements24 is seeking a skilled Pharmaceutical Clinical Research Associate (CRA) to join a globally integrated, fully remote team with operations extending to the Benoni area. This role monitors study sites, ensures data integrity, and protects patient safety throughout the trial lifecycle.

The ideal candidate has a Bachelor's degree in life sciences and at least 3 years of CRA experience, with strong knowledge of GCP/ICH and regulatory requirements.