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 correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
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 correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
trial to ensure protocol and GCP compliance
up to standard
Desirable additional education, work experience and personal abilities: Understanding of the challenges facing other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution
Desirable additional education, work experience and personal abilities: Understanding of the challenges facing other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution
ble additional education, work experience and personal abilities: