Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. This is your opportunity to join Rho as a Study Start Up Lead - we are open to this role being located in Italy, Spain, Poland, Latvia, Lithuania or Bulgaria. This is a remote opportunity. Responsibilities - Manage the study start up process through site activation, working with Project Manager and Clinical Trial Lead to ensure timely site activations - Participate in Sponsor meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics - Partner closely with both Functional Leads and SSU Team Members to proactively identify study start up related issues - Ensure that relevant systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level) - Provide operational oversight to SSU Associates on assigned projects - Responsible for all submissions and obtaining approval from IRB/ECs (incl CTIS Part 2 package); - May be responsible for submissions to Regulatory Authorities in non-EU countries (ex. UK, Georgia, South Africa etc)  - Coordinate feasibility efforts and work together with Clinical Team Leads on site identification - Identify the Site Essential Document (SED) packet elements required, agree with relevant internal staff, track the completion and upload of documents, and communicate with all parties (e.g., Sponsor, Site Staff, Internal Staff) the status of documents; participate as the SED Reviewer as necessary - Coordinate and develop the Start Up approach for IRB/EC approval at specified regional levels, including country level approval, and provide oversight of specific activities from SSU Team Members - Partner with Clinical Team Leads and the client to identify requirements for the Site Initiation Visit (SIV) and Site Activation - Coordinate the informed consent form (ICF) development, including the review, negotiation and approval with relevant internal and external parties - Support business development with proposal preparation and review and bid defense efforts - Coordinate site budget development, including the review, negotiation and approval with relevant internal and external parties. - Coordinate site contract negotiation process - Develop country/site-specific startup timelines and strategies and oversee startup activities in the country - Facilitate cooperation between cross-functional teams regarding startup activities

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. This is your opportunity to join Rho as a Study Start Up Lead - we are open to this role being located in Italy, Spain, Poland, Latvia, Lithuania or Bulgaria. This is a remote opportunity. Responsibilities - Manage the study start up process through site activation, working with Project Manager and Clinical Trial Lead to ensure timely site activations - Participate in Sponsor meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics - Partner closely with both Functional Leads and SSU Team Members to proactively identify study start up related issues - Ensure that relevant systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level) - Provide operational oversight to SSU Associates on assigned projects - Responsible for all submissions and obtaining approval from IRB/ECs (incl CTIS Part 2 package); - May be responsible for submissions to Regulatory Authorities in non-EU countries (ex. UK, Georgia, South Africa etc)  - Coordinate feasibility efforts and work together with Clinical Team Leads on site identification - Identify the Site Essential Document (SED) packet elements required, agree with relevant internal staff, track the completion and upload of documents, and communicate with all parties (e.g., Sponsor, Site Staff, Internal Staff) the status of documents; participate as the SED Reviewer as necessary - Coordinate and develop the Start Up approach for IRB/EC approval at specified regional levels, including country level approval, and provide oversight of specific activities from SSU Team Members - Partner with Clinical Team Leads and the client to identify requirements for the Site Initiation Visit (SIV) and Site Activation - Coordinate the informed consent form (ICF) development, including the review, negotiation and approval with relevant internal and external parties - Support business development with proposal preparation and review and bid defense efforts - Coordinate site budget development, including the review, negotiation and approval with relevant internal and external parties. - Coordinate site contract negotiation process - Develop country/site-specific startup timelines and strategies and oversee startup activities in the country - Facilitate cooperation between cross-functional teams regarding startup activities

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. This is your opportunity to join Rho as a Study Start Up Lead - we are open to this role being located in Italy, Spain, Poland, Latvia, Lithuania or Bulgaria. This is a remote opportunity. Responsibilities - Manage the study start up process through site activation, working with Project Manager and Clinical Trial Lead to ensure timely site activations - Participate in Sponsor meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics - Partner closely with both Functional Leads and SSU Team Members to proactively identify study start up related issues - Ensure that relevant systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level) - Provide operational oversight to SSU Associates on assigned projects - Responsible for all submissions and obtaining approval from IRB/ECs (incl CTIS Part 2 package); - May be responsible for submissions to Regulatory Authorities in non-EU countries (ex. UK, Georgia, South Africa etc)  - Coordinate feasibility efforts and work together with Clinical Team Leads on site identification - Identify the Site Essential Document (SED) packet elements required, agree with relevant internal staff, track the completion and upload of documents, and communicate with all parties (e.g., Sponsor, Site Staff, Internal Staff) the status of documents; participate as the SED Reviewer as necessary - Coordinate and develop the Start Up approach for IRB/EC approval at specified regional levels, including country level approval, and provide oversight of specific activities from SSU Team Members - Partner with Clinical Team Leads and the client to identify requirements for the Site Initiation Visit (SIV) and Site Activation - Coordinate the informed consent form (ICF) development, including the review, negotiation and approval with relevant internal and external parties - Support business development with proposal preparation and review and bid defense efforts - Coordinate site budget development, including the review, negotiation and approval with relevant internal and external parties. - Coordinate site contract negotiation process - Develop country/site-specific startup timelines and strategies and oversee startup activities in the country - Facilitate cooperation between cross-functional teams regarding startup activities

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. This is your opportunity to join Rho as a Study Start Up Lead - we are open to this role being located in Italy, Spain, Poland, Latvia, Lithuania or Bulgaria. This is a remote opportunity. Responsibilities - Manage the study start up process through site activation, working with Project Manager and Clinical Trial Lead to ensure timely site activations - Participate in Sponsor meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics - Partner closely with both Functional Leads and SSU Team Members to proactively identify study start up related issues - Ensure that relevant systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level) - Provide operational oversight to SSU Associates on assigned projects - Responsible for all submissions and obtaining approval from IRB/ECs (incl CTIS Part 2 package); - May be responsible for submissions to Regulatory Authorities in non-EU countries (ex. UK, Georgia, South Africa etc)  - Coordinate feasibility efforts and work together with Clinical Team Leads on site identification - Identify the Site Essential Document (SED) packet elements required, agree with relevant internal staff, track the completion and upload of documents, and communicate with all parties (e.g., Sponsor, Site Staff, Internal Staff) the status of documents; participate as the SED Reviewer as necessary - Coordinate and develop the Start Up approach for IRB/EC approval at specified regional levels, including country level approval, and provide oversight of specific activities from SSU Team Members - Partner with Clinical Team Leads and the client to identify requirements for the Site Initiation Visit (SIV) and Site Activation - Coordinate the informed consent form (ICF) development, including the review, negotiation and approval with relevant internal and external parties - Support business development with proposal preparation and review and bid defense efforts - Coordinate site budget development, including the review, negotiation and approval with relevant internal and external parties. - Coordinate site contract negotiation process - Develop country/site-specific startup timelines and strategies and oversee startup activities in the country - Facilitate cooperation between cross-functional teams regarding startup activities