Remote Senior Clinical Research Associate – Global Trials

Placements24; Pretoria; Hybrid; ZAR 700,000 - 950,000; Full time

Benefits offered by this job

Fully remote work

Company car or mileage reimbursement

Health, dental, and vision insurance

Professional development allowance

Retirement savings plan

Bonuses and incentives

Job summary

Placements24 partners with a global leader in clinical research to hire a Senior Clinical Research Associate. The role is fully remote, with travel to sites as needed, supporting studies managed in Pretoria, Gauteng.

You will monitor study conduct, ensure GCP compliance, and maintain data integrity while building strong relationships with investigative sites. Ideal candidates have 5+ years of CRA experience and proficiency with CTMS/EDC in global trials.

Qualifications

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate, with a strong track record in monitoring complex clinical trials.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience in therapeutic areas such as oncology, cardiology, or infectious diseases.
• Proficiency in CTMS and EDC systems.
• Excellent communication, interpersonal, and negotiation skills.
• Strong organizational and time-management abilities, with the capacity to manage multiple priorities.
• Willingness to travel domestically and internationally up to 60%.
• Remote work capability.

Responsibilities

• Conduct pre-study, initiation, interim monitoring, and close‑out visits for clinical trial sites.
• Ensure study conduct adheres to the clinical protocol, GCP, and all applicable regulations.
• Verify the accuracy, completeness, and quality of clinical data by reviewing source documents and CRFs.
• Manage and mentor site staff, providing training and support on study procedures.
• Oversee site performance and implement corrective actions as necessary.
• Prepare and submit monitoring visit reports in a timely manner.
• Manage investigational product accountability and drug dispensing at study sites.
• Liaise with investigators, site staff, and the clinical study team to resolve study-related issues.
• Ensure timely collection of essential study documents from investigational sites.
• Participate in study team meetings and contribute to study planning and strategy.
• Maintain a high level of expertise in relevant therapeutic areas and regulatory requirements.

Skills

Communication skills

Interpersonal skills

Negotiation skills

Organizational skills

Time management

Remote work

CTMS

EDC

Education

Bachelor's degree in life sciences or related field

Advanced degree preferred

Tools

CTMS

EDC

Job description

Placements24 partners with a global leader in clinical research to hire a Senior Clinical Research Associate. The role is fully remote, with travel to sites as needed, supporting studies managed in Pretoria, Gauteng.

You will monitor study conduct, ensure GCP compliance, and maintain data integrity while building strong relationships with investigative sites. Ideal candidates have 5+ years of CRA experience and proficiency with CTMS/EDC in global trials.