Pharmaceutical Clinical Research Associate (CRA)

Placements24; Bloemfontein; Híbrido; ZAR 600 000 - 900 000; Tempo integral

Resumo da oferta

Placements24 is seeking an experienced Pharmaceutical Clinical Research Associate to join a leading global CRO in Bloemfontein, Free State. The CRA will monitor clinical trial sites, verify data accuracy, and help ensure participant safety in line with GCP guidelines.

The role requires 3–5 years of CRA experience, strong ICH-GCP knowledge, and proficiency with CTMS and EDC systems. Expect travel up to 60% within the region and a central base for fieldwork.

Qualificações

• Bachelor’s degree in life sciences, nursing, pharmacy, or related field.
• Minimum 3–5 years as a Clinical Research Associate (CRA).
• Strong knowledge of ICH-GCP guidelines.
• Experience in site monitoring and managing multiple sites.
• Proficiency with CTMS and EDC systems.
• Excellent communication and organizational skills.

Responsabilidades

• Conduct site initiation, interim, and close‑out visits to clinical trial sites.
• Monitor trial progress, ensure adherence to protocol, GCP and regulatory requirements.
• Verify data accuracy by reviewing source documents and CRFs.
• Safely monitor adverse events and ensure timely reporting.
• Manage site product accountability and drug supplies.
• Train and support site staff on study procedures.
• Liaise between study sites and sponsor/CRO; prepare visit reports and escalate issues.
• Maintain comprehensive trial documentation.

Descrição da oferta de emprego

About the Role

Our client, a leading global Contract Research Organization (CRO), is seeking an experienced Pharmaceutical Clinical Research Associate (CRA) to join their expanding team in Bloemfontein, Free State. This role is pivotal in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines, protocols, and regulatory requirements. The CRA will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring patient safety. This is a fantastic opportunity for a dedicated clinical research professional to contribute to groundbreaking medical research in Bloemfontein, Free State, while working with a supportive and innovative organization. The Bloemfontein, Free State region is experiencing growth in the clinical research sector.

Key Responsibilities

• Conduct site initiation, interim, and close-out visits to clinical trial sites.
• Monitor clinical trial progress at assigned sites, ensuring adherence to protocol, GCP, and regulatory requirements.
• Verify the accuracy, completeness, and integrity of clinical trial data by reviewing source documents and case report forms (CRFs).
• Ensure the safety of study participants by monitoring adverse events and ensuring timely reporting.
• Manage site-level investigational product accountability and drug supplies.
• Train and support site staff on study-related procedures and requirements.
• Act as the primary liaison between the study sites and the sponsor/CRO.
• Prepare visit reports and **escalate** site issues to the clinical project manager as necessary.
• Maintain comprehensive and accurate study documentation.

Requirements

• Bachelor's degree in a life science, nursing, pharmacy, or a related scientific field.
• Minimum of 3-5 years of experience as a Clinical Research Associate, preferably within a CRO or pharmaceutical company.
• Thorough knowledge of ICH-GCP guidelines and applicable regulatory requirements.
• Proven experience in conducting site monitoring visits and managing multiple clinical trial sites.
• Excellent understanding of clinical trial processes and documentation.
• Strong organizational skills, attention to detail, and ability to manage time effectively.
• Excellent verbal and written communication skills, with the ability to build strong relationships with site personnel.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel frequently (up to 60%) within the assigned region.

Benefits

Our client offers a competitive salary, comprehensive medical and life insurance, a retirement savings plan, and performance-based bonuses. Opportunities for professional development include access to specialized training programs, career advancement pathways within the organization, and exposure to diverse therapeutic areas. This role provides the chance to be at the forefront of medical advancement, ensuring the integrity and success of vital clinical research. The Bloemfontein, Free State location offers a central base for fieldwork.