clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and data capturing correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment Notify relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and data capturing correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment Notify relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements
Analytical testing experience in a lab environment • Assist CEO to ensure business compliance policies and samples in the QC lab • Assist with investigating of internal and external NCRs • Assist with writing and revising