Senior Clinical Research Associate - Randburg

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

Benefits offered by this job

Health benefits

Bonuses

Career development opportunities

Job summary

Placements24 is seeking a Senior Clinical Research Associate to join our Randburg-based team to ensure trials comply with GCP and regulatory requirements.

You will monitor sites, manage data, train staff, and collaborate with investigators while supporting ongoing trial operations and quality assurance.

This role offers exposure to diverse therapeutic areas, a professional development track, and competitive benefits in a dynamic CRO setting.

Qualifications

• Bachelor's degree in life science, nursing, or related healthcare field.
• 4–5 years of CRA experience in pharma or CRO settings.
• In-depth knowledge of ICH-GCP and relevant regulations.
• Proven experience monitoring trials across multiple therapeutic areas.
• Strong site and data management understanding.
• Excellent organizational and communication skills.

Responsibilities

• Conduct site initiation, routine monitoring, and close-out visits per protocol and GCP.
• Verify data accuracy by reviewing CRFs and source documents.
• Maintain strong relationships with investigators and study staff.
• Ensure timely submission of essential documents and drug accountability.
• Identify deviations and escalate risks to project management.
• Assist in study document preparation and monitoring plan development.
• Train site personnel on procedures and data collection.
• Participate in investigator meetings and teleconferences.
• Contribute to risk-based monitoring strategies.

Skills

ICH-GCP knowledge

Site monitoring

Communication skills

Travel readiness

Education

Bachelor's degree in life science, nursing, or related healthcare field

Tools

CTMS

EDC systems

Job description

About the Role

Our client, a rapidly growing Contract Research Organization (CRO), is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated team, supporting operations in the Randburg, Gauteng area. This role is integral to the successful execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP), regulatory requirements, and study protocols. The Senior CRA will be responsible for site monitoring, data management, and fostering strong relationships with investigators and study staff. This is an exceptional opportunity for a seasoned clinical research professional to advance their career within a dynamic and supportive organization, contributing to the development of life-saving therapies.

Key Responsibilities

• Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with study protocols, GCP, and applicable regulations.
• Verify the accuracy, completeness, and integrity of clinical data by reviewing source documents and case report forms (CRFs).
• Manage communication and relationships with clinical trial sites, investigators, and study coordinators.
• Ensure timely submission of essential documents and proper drug accountability at study sites.
• Identify, document, and escalation study-related issues, deviations, and potential risks to project management.
• Assist in the preparation of study documents, including protocols, informed consent forms, and monitoring plans.
• Train site personnel on study procedures, protocols, and data collection requirements.
• Participate in investigator meetings and teleconferences as required.
• Contribute to the development and implementation of risk-based monitoring strategies.

Requirements

• Bachelor's degree in a life science, nursing, or a related healthcare field.
• A minimum of 4-5 years of experience as a Clinical Research Associate in pharmaceutical or CRO settings.
• In-depth knowledge of ICH-GCP guidelines and applicable regulatory requirements.
• Proven experience in monitoring clinical trials across various therapeutic areas.
• Strong understanding of clinical trial processes, including site management and data management.
• Excellent organizational, time management, and multitasking skills.
• Exceptional interpersonal and communication skills, with the ability to build rapport with site staff.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to clinical sites as required within the Randburg region and surrounding areas.
• Must be legally authorized to work in South Africa.

Benefits

Our client offers a competitive salary, comprehensive health and wellness benefits, performance-based bonuses, and extensive opportunities for professional development and career growth. You will join a respected CRO dedicated to advancing medical research and contributing to global health initiatives. This role offers a challenging and rewarding career within the vibrant business landscape of Randburg.