design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming challenges and work with the appropriate team leads to develop, resource and implement corrective measures
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming challenges and work with the appropriate team leads to develop, resource and implement corrective measures Actively activities and special projects Support the development of effective outreach strategies (e.g. Enhanced Support budget development with senior management, control and monitor expenditures of the clinic, adhering 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 challenges and work with the appropriate team leads to develop, resource and implement corrective measures Actively activities and special projects Support the development of effective outreach strategies (e.g. Enhanced Support budget development with senior management, control and monitor expenditures of the clinic, adhering of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
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
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