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SECTION 1: CONTACT DETAILS1A Lead Chief Investigator (Lead CI) Contact Details The Lead CI will be the primary contact and assumes responsibility for the project (see OCRF Guidelines) TitleFull NameDepartmentInstitutionAddressSuburbStatePostcodeOffice
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How to fill out roles in clinical trialsearly

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How to fill out roles in clinical trialsearly

01
Identify the various roles needed for the clinical trial, such as principal investigator, study coordinator, research assistant, data manager, and regulatory affairs specialist.
02
Determine the responsibilities and qualifications for each role.
03
Advertise the positions through job postings or recruitment agencies.
04
Screen and interview potential candidates for the roles.
05
Select the best candidates based on their qualifications and experience.
06
Provide training and orientation for the selected candidates on their specific roles and responsibilities.
07
Ensure clear communication and collaboration among the team members throughout the duration of the clinical trial.

Who needs roles in clinical trialsearly?

01
Researchers conducting clinical trials early in the process.
02
Sponsors and organizations funding and overseeing the clinical trials from the beginning.

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Roles in clinical trials refer to the specific responsibilities and functions of individuals involved in the clinical trial process, including investigators, coordinators, and sponsors.
Typically, sponsors and investigators of the clinical trials are required to file the roles in clinical trials.
Filling out roles in clinical trials generally involves providing information about the study, participants, and specific tasks or responsibilities assigned to each role.
The purpose of defining roles in clinical trials is to ensure that all participants understand their responsibilities and to maintain compliance with regulatory requirements.
Information that must be reported includes names of individuals assigned to roles, their qualifications, and specific responsibilities related to the clinical trial.
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