About the Role Our client, a global leader in pharmaceutical research and development, is seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to oversee clinical trials from their base in Kimberley, Northern Cape . This role is essential for ensuring the successful execution of clinical studies in accordance with protocol requirements, Good Clinical Practice (GCP), and all applicable regulatory guidelines. You will be responsible for site selection, initiation, monitoring, and close‑out activities, ensuring data integrity, patient safety, and timely trial progression. The ideal candidate will possess strong knowledge of clinical trial processes, excellent communication skills, and a meticulous approach to detail. Join our client's dedicated team in Kimberley and play a vital part in bringing innovative therapies to patients.
Key Responsibilities Identify, evaluate, and select potential clinical trial sites.
Initiate, monitor, and close‑out clinical trial sites according to study protocols and regulatory requirements.
Conduct site visits (on-site and remote) to verify data accuracy, ensure compliance with protocol and GCP, and assess patient safety.
Manage communication with investigators and site staff, addressing study‑related issues and providing necessary training.
Ensure timely submission of essential documents and accurate record‑keeping.
Prepare monitoring visit reports and follow up on action items.
Collaborate with internal study teams, including project managers, data managers, and medical monitors.




Contribute to the development of study‑related documents, such as monitoring plans and case report forms (CRFs).
Requirements 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 in the pharmaceutical industry.
In‑depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
Proven experience in site management, monitoring, and trial conduct.
Excellent interpersonal, communication, and negotiation skills.
Strong organizational skills with a high level of attention to detail.
Ability to work independently and manage multiple priorities effectively.
Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
Valid driver's license and willingness to travel extensively within the assigned region.
Benefits Our client offers a highly competitive salary and benefits package, including comprehensive health insurance, a retirement savings plan, and generous paid time off.
We provide excellent opportunities for professional development, including training on new technologies and methodologies, and support for professional certifications.
This role is based in Kimberley, Northern Cape , and offers a chance to work on impactful clinical trials that contribute to medical advancements.
Enjoy a agile work environment with a team dedicated to scientific excellence and patient well‑being.

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📌 Senior Clinical Research Associate (Pharmaceuticals) (British Columbia)
🏢 Placements24
📍 British Columbia