{"id":817,"date":"2021-03-22T16:47:41","date_gmt":"2021-03-22T20:47:41","guid":{"rendered":"https:\/\/mrctcenter.org\/individual-return-of-results\/?page_id=817"},"modified":"2021-03-22T16:47:41","modified_gmt":"2021-03-22T20:47:41","slug":"roadmap-by-role","status":"publish","type":"page","link":"https:\/\/mrctcenter.org\/return-of-individual-results\/how-to-return-irr\/roadmap-by-role\/","title":{"rendered":"IRR Roadmap By Role"},"content":{"rendered":"

[vc_row][vc_column][vc_empty_space][vc_column_text]Successful return of IRR can only come from the collaboration of all stakeholders within the clinical trial ecosystem. Different roles will have different priorities, concerns, and responsibilities.<\/p>\n

On the following pages we provide a roadmap for the IRR journey for specific stakeholders: Research sponsors, IRBs\/HRPPs, Study teams\/Site staff\/Investigators, and Patients\/Participants.<\/p>\n

These summaries are intended to be high-level reviews of the roles and responsibilities of each group, and they link\/refer to detailed guidance, tools, and case studies as applicable.[\/vc_column_text][\/vc_column][\/vc_row][vc_row equal_height=”yes”][vc_column width=”1\/2″][vc_cta h2=”Research Sponsors” txt_align=”center” style=”outline” add_button=”bottom” btn_title=”SEE ROADMAP” btn_style=”outline-custom” btn_outline_custom_color=”#2c4784″ btn_outline_custom_hover_background=”#2c4784″ btn_outline_custom_hover_text=”#ffffff” btn_shape=”round” btn_align=”center” add_icon=”top” i_icon_fontawesome=”fas fa-building” i_color=”custom” i_background_style=”rounded” i_on_border=”true” btn_link=”url:https%3A%2F%2Fmrctcenter.org%2Freturn-of-individual-results%2Fhow-to-return-irr%2Froadmap-by-role%2Fsponsors%2F|title:Sponsors” i_custom_color=”#2c4784″]Those developing treatments and financing clinical trials.[\/vc_cta][\/vc_column][vc_column width=”1\/2″][vc_cta h2=”IRBs\/HRPPs” txt_align=”center” style=”outline” add_button=”bottom” btn_title=”SEE ROADMAP” btn_style=”outline-custom” btn_outline_custom_color=”#2c4784″ btn_outline_custom_hover_background=”#2c4784″ btn_outline_custom_hover_text=”#ffffff” btn_shape=”round” btn_align=”center” add_icon=”top” i_icon_fontawesome=”fas fa-balance-scale-left” i_color=”custom” i_background_style=”rounded” i_on_border=”true” btn_link=”url:https%3A%2F%2Fmrctcenter.org%2Freturn-of-individual-results%2Fhow-to-return-irr%2Froadmap-by-role%2Firb-hrpp%2F|title:Sponsors” i_custom_color=”#2c4784″]Those providing ethical reviews of research or managing human research protections programs.[\/vc_cta][\/vc_column][\/vc_row][vc_row equal_height=”yes”][vc_column width=”1\/2″][vc_cta h2=”Investigators, Study\/Site Staff” txt_align=”center” style=”outline” add_button=”bottom” btn_title=”SEE ROADMAP” btn_style=”outline-custom” btn_outline_custom_color=”#2c4784″ btn_outline_custom_hover_background=”#2c4784″ btn_outline_custom_hover_text=”#ffffff” btn_shape=”round” btn_align=”center” add_icon=”top” i_icon_fontawesome=”fas fa-microscope” i_color=”custom” i_background_style=”rounded” i_on_border=”true” btn_link=”url:https%3A%2F%2Fmrctcenter.org%2Freturn-of-individual-results%2Fhow-to-return-irr%2Froadmap-by-role%2Fresearch-site-study-staff-and-pis%2F|title:Sponsors” i_custom_color=”#2c4784″]Principal Investigators, study team members, and staff at research sites.[\/vc_cta][\/vc_column][vc_column width=”1\/2″][vc_cta h2=”Patients\/Participants” txt_align=”center” style=”outline” add_button=”bottom” btn_title=”SEE ROADMAP” btn_style=”outline-custom” btn_outline_custom_color=”#2c4784″ btn_outline_custom_hover_background=”#2c4784″ btn_outline_custom_hover_text=”#ffffff” btn_shape=”round” btn_align=”center” add_icon=”top” i_icon_fontawesome=”fas fa-user-circle” i_color=”custom” i_background_style=”rounded” i_on_border=”true” btn_link=”url:https%3A%2F%2Fmrctcenter.org%2Freturn-of-individual-results%2Fhow-to-return-irr%2Froadmap-by-role%2Fparticipants%2F|title:Participants” i_custom_color=”#2c4784″]Those participating in or considering clinical trials, and their family members\/caregivers.[\/vc_cta][\/vc_column][\/vc_row]<\/p>\n<\/section>","protected":false},"excerpt":{"rendered":"

[vc_row][vc_column][vc_empty_space][vc_column_text]Successful return of IRR can only come from the collaboration of all stakeholders within the clinical trial ecosystem. Different roles will have different priorities, concerns, and responsibilities. On the following pages we provide a roadmap for the IRR journey for specific stakeholders: Research sponsors, IRBs\/HRPPs, Study teams\/Site staff\/Investigators, and Patients\/Participants. These summaries are intended to […]<\/p>\n","protected":false},"author":5,"featured_media":0,"parent":986,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"template-sub.php","meta":{"footnotes":""},"class_list":["post-817","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nIRR Roadmap By Role - Return of Individual Research Results<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/mrctcenter.org\/return-of-individual-results\/how-to-return-irr\/roadmap-by-role\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"IRR Roadmap By Role\" \/>\n<meta property=\"og:description\" content=\"[vc_row][vc_column][vc_empty_space][vc_column_text]Successful return of IRR can only come from the collaboration of all stakeholders within the clinical trial ecosystem. 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