trial to ensure protocol and GCP compliance
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
up to standard
ired minimum work experience:
Social Sciences Required minimum work experience: 5 to 8 years' experience in a middle management role in the Management Experience working in a managerial role at a health care center or clinic Extensive experience working donor funded programmes Experience with management of multiple stakeholders Experience in data analysis and evaluation Desirable additional education, work experience and personal abilities: Understanding of the transgender people in community settings Previous experience in Sexual Reproductive Health (SRH) services
Social Sciences Required minimum work experience: 5 to 8 years' experience in a middle management role in the Management Experience working in a managerial role at a health care center or clinic Extensive experience working donor funded programmes Experience with management of multiple stakeholders Experience in data analysis and evaluation Desirable additional education, work experience and personal abilities: Understanding of the transgender people in community settings Previous experience in Sexual Reproductive Health (SRH) services