Clinical Research Associate - Hybrid

Placements24; Kempton Park; Hybrid; ZAR 400,000 - 700,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Placements24 is seeking a dedicated Clinical Research Associate (CRA) to join a growing pharmaceutical team in Gauteng. This hybrid role blends remote flexibility with essential on-site collaboration to support clinical trials and ensure data quality and regulatory compliance.

The successful candidate will monitor sites, verify data, train staff, and coordinate with sponsors across SA. Travel up to 50% is required. A life-science degree and at least 3 years of CRA experience are preferred.

Qualifications

• Bachelor's degree in life science, nursing, or related field.
• ≥3 years in CRA or similar clinical trial monitoring role.
• Thorough ICH-GCP knowledge and regulatory awareness.
• Experience in site visits: initiation, monitoring, close-out.
• Proficient with EDC and CTMS systems.
• Excellent organizational and time-management skills.
• Strong interpersonal and communication abilities; builds rapport.
• Willingness to travel ~50%.
• Hybrid work model capability.

Responsibilities

• Monitor trial activities at sites to ensure protocol/SOP/regulatory compliance.
• Verify data accuracy via source data verification.
• Serve as primary contact between sponsor and sites.
• Ensure investigational product handling per protocol and regs.
• Oversee site recruitment, enrollment, retention.
• Report deviations from protocol, GCP, SOPs.
• Train site personnel on procedures and data collection.
• Participate in site initiation, monitoring, close-out visits.
• Prepare and submit monitoring visit reports in a timely manner.
• Contribute to study documents development and review.

Skills

Bachelor's degree in life science or相关

3+ years CRA experience

ICH-GCP knowledge

Site monitoring experience

EDC proficiency

CTMS proficiency

Organizational skills

Communication skills

Willingness to travel 50%

Hybrid work capability

Education

Bachelor's degree in life science

Tools

EDC systems

CTMS

Job description

About the Role

Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding pharmaceutical team in Tembisa, Gauteng . This hybrid role offers a blend of remote flexibility and essential on-site collaboration, allowing you to contribute effectively to vital clinical trials. You will be responsible for ensuring the quality, integrity, and accuracy of data collected during clinical investigations, adhering strictly to study protocols, and complying with Good Clinical Practice (GCP) guidelines. This position is crucial for the successful execution of our clinical development programs, helping to bring life-changing therapies to patients. The role requires a proactive approach to monitoring study progress, site management, and regulatory compliance, making it an integral part of our research and development efforts. The successful candidate will play a key role in advancing pharmaceutical innovation within the region.

Key Responsibilities

• Monitor clinical trial activities at assigned investigative sites to ensure adherence to protocols, SOPs, and regulatory requirements.
• Verify the accuracy, completeness, and validity of clinical data through source data verification.
• Serve as the primary point of contact between the sponsor and the investigative sites, fostering strong working relationships.
• Ensure investigational product is managed appropriately according to protocol and regulations.
• Oversee site recruitment, patient enrollment, and retention efforts.
• Identify, document, and report any deviations from protocol, GCP, or SOPs.
• Train site personnel on study procedures, data collection, and regulatory compliance.
• Participate in site initiation, monitoring, and close-out visits.
• Prepare and submit monitoring visit reports in a timely manner.
• Contribute to the development and review of study-related documents.

Requirements

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
• Demonstrated experience in conducting site visits, including initiation, monitoring, and close-out.
• Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational, time management, and problem-solving skills.
• Strong interpersonal and communication skills, with the ability to build rapport with site staff and colleagues.
• Ability to travel to investigative sites as required (approximately 50% travel).
• Detail-oriented with a commitment to data integrity and patient safety.
• Must be able to work effectively in a hybrid model, balancing remote work with on-site responsibilities.

Benefits

Our client offers a competitive salary and a comprehensive benefits package. This includes medical, dental, and vision insurance, a retirement savings plan with company matching, and paid time off. Opportunities for professional development and continued education are provided to support career growth. Employees will have access to modern office facilities for on-site work and a supportive team environment. The hybrid model allows for greater flexibility in managing personal and professional commitments. We believe in recognizing and rewarding the contributions of our employees, fostering a culture of appreciation and collaboration within the Tembisa area.