Empower & Elevate your research team's expertise with Wits Health Consortium's comprehensive training program designed for principal and sub-investigators, as well as senior research team members. Our training covers:
Developing Research Protocols: Master the use of precise terminology and craft clear, effective research protocols.
Ethical and Participant Safety: Learn to prioritize ethics and ensure the highest standards of participant safety.
Investigational Product Development: Gain a deep understanding of the investigational product development process and navigate regulatory requirements seamlessly.
Clinical Trial Operations: Familiarize yourself with the ins and outs of clinical trial operations and your specific responsibilities.
Study and Site Management: Enhance your skills in managing study and site activities to ensure smooth operations.
Creating Essential Documents: Learn to produce accurate and integral study documents that uphold data quality.
Monitoring and Audits: Handle monitoring, audit, and inspection visits with confidence and expertise.
Team Roles and Delegation: Identify and delegate tasks effectively within your study team to streamline workflow.
Effective Communication: Utilize advanced communication methods and tools to foster teamwork and collaboration.
Equip your team with the knowledge and skills to excel in every facet of research management. Join Wits Health Consortium for this essential training in Parktown, Gauteng, and drive your clinical research site to success.
HPSCA CPD Points : 30
Cost:
R 6,900 Incl VAT
Group Discounts can be negotiated
The programme curriculum includes the following modules:
1. Scientific Concepts and Research Design
2. Ethical and Participant Safety Considerations
3. Investigational Product Development
4. Clinical Trial Operations
5. Study and Site Management
6. Data Management & Informatics
7. Professionalism & Leadership
8. Communication & Teamwork
Online Learning: Learners will be given access to the eLearning platform after registering for the programme. All pre-reading, post reading, assignments, assessments, lessons and resources will be hosted on an eLearning platform.
Learning Material: Learners will be provided with a Clinical Research Education Programme workbook. The workbook contains detailed information about all the topics covered during the in class as well as the eLearning sessions.
eLearning PlatformAdministered: Course sessions on the eLearning platform will followthe same index as the in class sessions, and studentshave to complete the related course session on theeLearning platform before attending the in classsession with the same session number.