responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable protocols
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 minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education to protocols Exceptional organizational and administrative skills are required together with working knowledge
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 minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education to protocols Exceptional organizational and administrative skills are required together with working knowledge
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement programme
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming 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 Perform and comply with administrative procedures associated with accurate clinical record keeping and reporting and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming 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 Perform and comply with administrative procedures associated with accurate clinical record keeping and reporting and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
including operating systems, security tools, applications, servers, email systems, laptops, desktops, such as attending to staffing requirements and administration