concerns affecting our region, including HIV and its related problems, sexual and reproductive health, and vaccinology responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor in a Health-Related Field Required minimum work experience: 3-5 years experience in clinical trials/research
concerns affecting our region, including HIV and its related problems, sexual and reproductive health, and vaccinology responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor in a Health-Related Field Required minimum work experience: 3-5 years experience in clinical trials/research
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Required minimum experience:
Desirable
concerns affecting our region, including HIV and its related problems, sexual and reproductive health, and vaccinology design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming Regularly monitor and track site performance in relation to programme targets Anticipate implementation management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring
concerns affecting our region, including HIV and its related problems, sexual and reproductive health, and vaccinology design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming Regularly monitor and track site performance in relation to programme targets Anticipate implementation management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming team
requirements are met