clinical trial activities according to good clinical practice, the study protocol, and the site's standard operating 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
clinical trial activities according to good clinical practice, the study protocol, and the site's standard operating 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
clinical trial activities according to good clinical practice, the study protocol, and the site's standard trial to ensure protocol and GCP compliance
other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution
other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution
up to standard