Plan, arrange and conduct monitoring visits for assigned research studies according to monitoring plan and ensure compliance towards the relevant protocols, guidelines and regulatory requirement
Collection and transcription of study patient data into case report forms
Act as intermediary between services and departments while overseeing data and specimen management
Writing of post-visit monitoring report and recommend actions for areas of non-compliance
Liaise with internal stakeholders to perform timely submissions for regulated and non-regulated research studies
Organize training activities to educate research study teams to promote awareness of the regulatory responsibilities as well as the culture of proper conduct of research
Provide regulatory advice to stakeholders
Collect and compile data for management reporting
Requirements
Min Dip/Deg in any discipline
1-2 years experience in clinical/lab coordinator will be advantageous
Meticulous and efficient
Knowledge of Microsoft Excel
Excellent communication skills
If you are interested in any of the positions, do kindly drop your most updated resume to victoriayam@recruitexpress.com.sg
Healthcare / Pharmaceutical / Life Science / Medical Device
Specialization
Healthcare - Nurse / Allied Healthcare Healthcare - Pharmaceutical / Life Science / Medical Device / Clinical Research / Regulatory Affairs
Location
Central
Employment Type
Permanent
Salary
Negotiable
If you meet the requirements of this role, please email a detailed resume in Word document to Victoria Yam Wen Ting. CEI Registration No.: R21103142 Email: victoriayam@recruitexpress.com.sg Tel: 67363280 *All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.
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