Use the information below to understand each site role and select the role that best aligns with an individual's responsibilities at the study site.
Administrative:
An individual primarily responsible for supporting administrative activities including but not limited to, management of resources, oversight of staff, maintaining study operations, and marketing and patient recruitment.
Clinical:
An individual responsible for providing clinical operations at the site.
Lab:
An individual primarily responsible for performing laboratory tests or processing samples, (e.g., HLA-typing, blood-typing, PBMC processing).
Pharmacy:
The individual responsible for managing the preparation and dispensation of the study product/ device.
Principal Investigator:
The individual who actually conducts the clinical investigation (i.e., under whose immediate direction the drug is administered or dispensed to a subject) at the approved site. In the event an investigation is conducted by a team of individuals, the investigator is the responsible leader of the team.
Quality Management:
An individual primarily responsible for conducting quality assurance activities at a site.
Regulatory:
An individual primarily responsible for handling submissions to the Sponsor, regulatory body, or IRB/EC for the study.
Study Coordinator:
An individual responsible for the management and coordination of a protocol for the study site under the guidance of the principal investigator.
Sub-Investigator:
Any individual member of the clinical study team designated and supervised by the investigator and provide a direct and significant contribution to the data. For DMID, this would include those assessing safety and eligibility of participants.
Other:
An individual providing support to a study or site that does not belong in any of the above categories.