As a Study Coordinator Intern, you will assist with the coordination of clinical trials under the supervision and guidance of the host site team to ensure that all clinical trials are managed according to the International Conference for Harmonization (ICH) guidelines for Good Clinical Practice (GCP) and maintain the safety and protection of trial participants and the integrity of trial data subsequently collected.
Postdoctoral academic research role
This internship is not a postdoctoral academic research role, however, you will be working with renowned clinicians in their field, learning about the clinical trials research environment and the different stakeholders involved. You will acquire a breadth of knowledge and skills that will equip you to progress a career in clinical trials/clinical research after the internship.
Writing trial protocols and publishing
Interns will not be involved in writing or publishing trial protocols. Trial protocols are written by trial sponsors: commercial, collaborative group or investigator initiated. However, you or your team may be acknowledged in clinical trials publications authored by the main trial investigator.
After the internship, you may end up with a career in research project management (leading project planning and managing a team responsible for the project's delivery from ideation through to completion), where you may assist investigators in writing trial protocols for investigator-initiated trials. But this is not something to expect within the internship period.
Being a clinical trial investigator
Interns do not perform the role of a Clinical Trial Investigator. To be an investigator, you must have the medical background and expertise required to oversee and manage trial patients. Although you are not an investigator, you will be part of a collaborative research team, working alongside renowned clinicians and experts in cancer clinical trials. You will also be exposed to innovative research ideas and treatment breakthroughs in cancer research.
Conducting clinical assessments
Interns do not conduct clinical assessments of trial participants, which requires an appropriate medical background. However, you will be able to manage and coordinate the patient treatment journey while on trials, by liaising with a multidisciplinary clinical team. You will be able to learn about the hospital environment and healthcare system in Australia.
You may end up with a career in research project management (leading project planning and managing a team responsible for the project's delivery from ideation through to completion). after the internship, where you may assist investigators in writing trial protocols for investigator-initiated trials. But this is not something to expect within the internship period.
A host site is best described as a Victorian hospital or health service participating in the SKILLED internship program. To learn more about The Royal Children’s Hospital which is one of the host sites, watch this video: https://www.youtube.com/watch?v=2T1kLq3I8w4
Host sites complete an expression of interest and provide detailed site information, so VCCC Alliance can ensure high standards of training and supervision are maintained. This also ensures the intern receives the necessary experience across all areas of the required competencies. There are many host sites that have been consistently involved with the program since 2019.
Matching interns to sites are based on many factors, including knowledge, size and structure of the of the unit within the site, applicant’s previous experience, career aspirations and geographic location.
Interns are matched to sites by an expert panel, with applicant preferences and personal circumstances considered. All sites have been deemed suitable to ensure the best possible internship and training experience. The intern is not obliged to accept the placement location offered, however due to the complexity involved with matching interns, an alternative may not be available.
A small number of placements are on a rotation / shared placement arrangement, but most placements are at one site for the duration of placement. If you are going to be offered a rotational placement, this will be discussed with the applicant. One-week optional rotation through PPCU is available for interns unable to gain experience in all areas of the SC competency assessment at their host site.
No. All training outlined will be covered by the VCCC Alliance.
A scholarship is provided, as a stipend (over 40 weeks) to the equivalent of $36,000 for Study Coordinator interns.
Yes. Vaccination requirements for interns are the same as all healthcare professionals in the health care sector in line with Victorian Government policy: https://www2.health.vic.gov.au/public-health/immunisation/adults/vaccination-workplace/vaccination-healthcare-workers
If successful in being offered placement, these checks will be conducted in accordance with site policy, prior to commencement at site.
Yes. Regionally placed interns will be reimbursed costs of pre-approved expenses to return to Melbourne for in-person mandatory training.
As interns are not employees, there is no leave entitlement as such. However, interns are permitted a total of five days unplanned absence (in relation to illness/unforeseen emergencies) during the internship. Interns are not required to attend placement on Victorian Public Holidays. Interns can also access five days planned absence, in consultation with their placement site. This is encouraged to occur mid-way through the placement.
The intern is responsible for attending the Host Site and receiving skills training from the Host to meet the training requirements and Competency Framework and complete the Competency Assessment. Details of attendance: Monday – Friday between the hours of 8am and 5pm.
No
For questions not addressed in the FAQ, or in the recruitment information on this website or SEEK, please contact us at [email protected]
