Become a Practicum Host
Each year, Western Continuing Studies invites clinical trials professionals to host post-degree diploma students for the practicum component of the Diploma in Clinical Trials Management. We work with you and our students to coordinate the best possible professional practicum placement for the applicant and organization.
The Diploma in Clinical Trials Management is a post-degree program that includes 9 diploma-credit courses plus a student practicum for which the student receives academic credit. Students are eligible to apply to the Diploma in Clinical Trials Management only after successful completion of an undergraduate degree from an accredited university.
The practicum is the final term of the Diploma in Clinical Trials Management. Students must complete 400 hours at their practicum site between May 1, 2018 and August 31, 2018 (exact end date may vary slightly). During this period, students are expected to be on site on a full-time basis (i.e. 22 hours per week).
The key dates for our 2017-2018 practicum process are:
|Jan 26||Deadline to submit a posting|
|Feb 5 - 9||Students will submit their applications to sites by email|
|Feb 12 - Mar 16||Interview period|
|May 1 - Aug 31||Practicum period|
There is not a prescribed list of activities that must be completed. Instead, the Practicum Supervisor helps the student to create six learning goals for the four month practicum based on the student’s interests, and current projects at the site.
Requirements of Practicum Supervisors
As students’ skills are at an entry level, supervision, explanation, and direction are vital. The student’s supervisor should be a practitioner who has at least 3 years of relevant clinical trials experience. Although the student can be expected to work fairly independently, contact and supervision is expected from the supervisor.
The Role of the Practicum Supervisor
- Help the student to create six learning goals for the practicum; evaluate their performance in meeting the goals at the end of the practicum
- Review weekly journal entries submitted by the student; evaluate the student’s performance in reflecting in their journal at the end of the practicum
- Meet with the student once per week to discuss their progress and provide feedback
- Provide the student with a range of experience in as many aspects of clinical trials as possible
- Orient the student to the clinical trial function in the organization, including policies, procedures and personnel
- Monitor work assignments and provide constructive feedback
- Be available and accessible for counsel and advice
- Provide the student with networking opportunities
- Introduction to Clinical Trials and Research
- Drug Development
- Organization and Monitoring of Clinical Trials I
- Reading and Understanding Research Information
- Regulatory, Legal and Ethical Issues of Clinical Trials
Through the course work, students have developed knowledge in:
- The historical background of the laws governing drug development (FDA Regulations)
- The key regulations that impact the development of drugs
- The types of clinical trial designs
- The place of allied health in health research
- The terminology and definitions used in clinical trials
- The laws that govern the drug approval process
- The interpretation of safety and efficacy data
- Strategies for organizing clinical trials and site management to ensure a successful outcome
- The principles of ICH GCP responsibilities in the clinical trial process
- The importance of Good Clinical Practice Guidelines (GCP) and International Clinical Conference on Harmonization (ICH) ethics of clinical trials
Submit a Posting
Contact Heather Wakely with the following information:
- Name and email address
- Learning opportunities
- Skills required/valued
- Information regarding payment, honorarium, professional development opportunities, etc. (if applicable)
Looking forward to partnering with you during the upcoming year!