Hybrid Clinical Research Associate - Bloemfontein

Placements24

Bloemfontein

Hybrid

ZAR 420,000 - 650,000

Full time

7 days ago

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Benefits offered by this job

Health benefits

Paid time off

Professional development

Hybrid work model

Job summary

Placements24 is seeking a dedicated Clinical Research Associate to join our clinical operations team in the Bloemfontein region, with hybrid work flexibility. You will monitor trial sites to ensure studies are conducted, recorded, and reported in line with protocol, SOPs, and GCP guidelines, ensuring patient safety and data integrity.

The ideal candidate has a life sciences degree, at least 3 years of CRA or monitoring experience, and strong communication skills.

Qualifications

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related discipline.
Minimum of 3 years of experience as a Clinical Research Associate or equivalent monitoring role.
Thorough understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.

Responsibilities

Conduct site initiation, interim monitoring, and close-out visits in accordance with study requirements and GCP.
Verify the accuracy and completeness of source data and ensure its consistency with the Case Report Forms (CRFs).
Ensure compliance with the study protocol, regulatory requirements, and SOPs at assigned clinical sites.
Manage communication between the investigative sites and the clinical trial team.
Oversee site compliance, review regulatory binders, and ensure proper investigational product accountability.
Identify and elevate any site-level issues or protocol deviations to the project manager.