Clinical Trial Site Coordination
Subject CLRS90022 (2011)
Note: This is an archived Handbook entry from 2011.
| Credit Points: | 12.50 | ||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Level: | 9 (Graduate/Postgraduate) | ||||||||||||||||||||||||
| Dates & Locations: | This subject has the following teaching availabilities in 2011: Semester 1, Hawthorn - Taught on campus.
Semester 2, Hawthorn - Taught on campus.
Face-to-Face Lecture Timetable can be viewed here. For information about these dates, click here. | ||||||||||||||||||||||||
| Time Commitment: | Contact Hours: 24 hours Total Time Commitment: Estimated total time commitment of 160 hours. | ||||||||||||||||||||||||
| Prerequisites: | nil | ||||||||||||||||||||||||
| Corequisites: | nil | ||||||||||||||||||||||||
| Recommended Background Knowledge: | nil | ||||||||||||||||||||||||
| Non Allowed Subjects: | nil | ||||||||||||||||||||||||
| Core Participation Requirements: | For the purposes of considering requests for Reasonable Adjustments under the Disability Standards for Education (Cwth 2005), and Students Experiencing Academic Disadvantage Policy, academic requirements for this subject are articulated in the Subject Description, Subject Objectives, Generic Skills and Assessment Requirements of this entry. The University is dedicated to provide support to those with special requirements. Further details on the disability support scheme can be found at the Disability Liaison Unit website: http://www.services.unimelb.edu.au/disability/ |
Contact
Melbourne Consulting and Custom Programs
Level 3, 442 Auburn Rd
Hawthorn VIC 3122
Phone: 9810 3185
Email: clinicalresearch@mccp.unimelb.edu.au
| Subject Overview: |
In this subject, students will select a minimum of 10 hours of electives depending on their needs plus a compulsory capstone component. Electives (minimum of 10 hours of teaching). Capstone |
|---|---|
| Objectives: | Students who successfully complete this subject will: • Understand how to effectively coordinate research activities at a clinical research site • Understand and manage risk at a clinical research site • Understand the role of project management in good clinical practice • Be able to provide input in the implementation of clinical research studies within Australia • Understand the purpose and operational responsibilities of a Clinical Research Associate in maintaining the quality standards defined by Australian legislation and Good Clinical Practice |
| Assessment: |
Assessment for this subject will be based around the individual modules, plus an overall assessment of the content of the two subjects. This will comprise: • 2,000 word assignments for the electives, with a total contribution of 40% of the marks for the subject. Each assessment piece is due four weeks after the relevant lecture. Students must achieve a mark of at least 50% in each of the assessments to achieve a pass grade for this subject. |
| Prescribed Texts: | nil |
| Recommended Texts: | NA |
| Breadth Options: | This subject is not available as a breadth subject. |
| Fees Information: | Subject EFTSL, Level, Discipline & Census Date |
| Generic Skills: |
• Risk management • Project management |
| Links to further information: | www.mccp.unimelb.edu.au |
| Related Course(s): |
Specialist Certificate in Clinical Research-Clinical Trials Coordination |
Download PDF version.