Publié le 8 novembre 2026 · Expire le 15 novembre 2026
Description du poste
• Coordinate and support daily clinical trial activities, including patient recruitment, screening, enrolment and follow-up.
• Assist with patient appointments, study visits and collection of clinical trial data.
• Maintain accurate clinical trial documentation, records and study files in compliance with study protocols and regulatory requirements.
• Liaise with doctors, nurses, patients and research teams to ensure smooth coordination of clinical trials.
• Assist with preparation for study audits, monitoring visits and regulatory submissions when required.
Requirements:
• Diploma in Life Sciences, Biomedical Science, Nursing, Pharmacy or a related discipline.
• Good organisational and administrative skills with strong attention to detail.
• Good communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Coordinate and support daily clinical trial activities, including patient recruitment, screening, enrolment and follow-up.
• Assist with patient appointments, study visits and collection of clinical trial data.
• Maintain accurate clinical trial documentation, records and study files in compliance with study protocols and regulatory requirements.
• Liaise with doctors, nurses, patients and research teams to ensure smooth coordination of clinical trials.
• Assist with preparation for study audits, monitoring visits and regulatory submissions when required.
Requirements:
• Diploma in Life Sciences, Biomedical Science, Nursing, Pharmacy or a related discipline.
• Good organisational and administrative skills with strong attention to detail.
• Good communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
If you are keen to apply for the position, kindly email your detailed resume in MS Word to hr@recruit-expert.com
Please note that only shortlisted candidates will be notified.
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EA Licence: 19C9701
Registration: R1326740