responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Required minimum education and training:
Desirable additional education, work experience
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 Manage and support staff members Required minimum education and training: Degree or Honours Degree in a Health-Related 3-5 years experience in clinical trials/research Desirable additional education, work experience, and personal
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 Manage and support staff members Required minimum education and training: Degree or Honours Degree in a Health-Related 3-5 years experience in clinical trials/research Desirable additional education, work experience, and personal
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 administrative procedures associated with accurate clinical record keeping and reporting including patient 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 administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
Radiologists, Anaesthetists, Nephrologists, ICU & Ward Nurses, Theatre & Scrub Sisters, Pharmacy Managers from Our Client. Supply hospitals, physicians, clinical and homecare staff with current product information for tenders. Provide in-service educational seminars for the clinical staff of hospitals, including face
related field, registered Skills Development Facilitator
At least 5 years of in instructional design, accreditation, and facilitation
necessary contributions from various departments and facilitate their collaboration Work alongside project management architecture Ability to work with various departments to facilitate the orderly execution of a proposed project plan
in instructional design, accreditation, and facilitation Reporting analytics and administration SDF Functionalities: practices in training methodologies Design and facilitate instructional training sessions Handle reporting in instructional design, accreditation, and facilitation Proficient in reporting, analytics, and administration