Rho, an award-winning, stable, full-service CRO known for its collaborative, dynamic culture based in the US, is quickly expanding their presence in Europe. We are a thriving company, and we will deliver global full-service clinical development services and unmatched customer support – worldwide. Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. As a Sr. CRA, you will be a key player in our innovative team, dedicated to ensuring that our clinical trials are conducted with the utmost integrity and quality. Your expertise will help us navigate the complexities of clinical research as we strive to deliver meaningful solutions to healthcare challenges. The Clinical Monitoring team at Rho is known for its collaborative spirit and commitment to excellence. Join us to not only advance your career but also contribute to a culture that celebrates innovation, supports professional growth, and values every team member's input. This is a permanent Senior CRA role to be home based role in Poland. Responsibilities: - May contribute to the development of study tools and materials as well as documentation for clinical trials - May provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members - May provide support to the RFP process - Prepare and perform all onsite & off-site/remote site monitoring visit activities across multiple protocols, inclusive of all study visit types as needed (SQV, SIV, IMV and COV), according to Good Clinical Practice (GCP), Protocol, applicable regulations and Sponsor requirements under supervision of experienced staff - Effectively documents observations in site visit reports and follow up letters within timelines required by Rho’s procedural documents and the applicable clinical monitoring plan - Prepare (if needed) and maintain Investigator Site Files (ISF), and maintain site binders and documents of the TMF (Trial Master - May assist in payment processes, including liaison with Site and review Site and patient data for visits being invoiced - Assist in the appropriate identification and action of AE (Adverse Event), SAEs (Serious Adverse Event) and pregnancy reporting procedure - Verify and confirm appropriate IMP (Investigational Medicinal Product) handling at Site and perform drug accountability - Help to plan and perform Country and Site Feasibility, including assessment of potential Risks and challenges, as well as select Study sites and perform pre-study visits - Assist in selection of Study specific Vendors and perform Vendor assessments - Support in negotiation and execution of Investigator/ Institution contracts - May help to prepare documents submission to Ethics Committee, Competent Authorities and other bodies (as applicable), including communication with Sponsor, EC/ CA and other involved parties For Senior CRAs: - Provide mentoring, training, and co-monitoring of junior CRAs and other clinical team members. - May support Clinical Team Lead and Project Management tasks on assigned studies as-requested (e.g. study specific process development, trip report review, newsletter creation, leading CRA project team calls, etc.) - May conduct sign-off visits to assess competency of other CRAs - May attend and present at meetings and conferences, including Investigator Meetings - May participate in the interview and selection process for CRAs

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. We are currently hiring an In-House Clinical Research Associate to join our team! As an In-House CRA here at Rho, you’ll have the opportunity to gain the necessary experience to grow into a traveling Clinical Research Associate (CRA) and work with the Project Manager, traveling CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed. You’ll manage data entered into the CTMS (clinical trials management system) and other project tracking tools. You’ll also assist CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations. You may also have the opportunity to mentor other team members. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing: - Collect, track and review investigational site records relating to subject screening and enrollment - Assist in the development of study plans and status reports - Collect, track, and review all site regulatory documents - Assist with development and review of Informed Consent Forms - Interact with sites, clients, vendors and internal study team members - Maintain the clinical trials management system (CTMS) and other project tracking tools - Track study supplies and coordinate shipments of supplies to sites as needed - Manage the study Trial Master File (TMF) and ensure periodic TMF audits - Coordinate work with CRAs monitoring on-site - Perform on site co-monitoring and remote monitoring activities - Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines

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. We are currently hiring an In-House Clinical Research Associate to join our team! As an In-House CRA here at Rho, you’ll have the opportunity to gain the necessary experience to grow into a traveling Clinical Research Associate (CRA) and work with the Project Manager, traveling CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed. You’ll manage data entered into the CTMS (clinical trials management system) and other project tracking tools. You’ll also assist CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations. You may also have the opportunity to mentor other team members. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing: - Collect, track and review investigational site records relating to subject screening and enrollment - Assist in the development of study plans and status reports - Collect, track, and review all site regulatory documents - Assist with development and review of Informed Consent Forms - Interact with sites, clients, vendors and internal study team members - Maintain the clinical trials management system (CTMS) and other project tracking tools - Track study supplies and coordinate shipments of supplies to sites as needed - Manage the study Trial Master File (TMF) and ensure periodic TMF audits - Coordinate work with CRAs monitoring on-site - Perform on site co-monitoring and remote monitoring activities - Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines

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. We are currently hiring an In-House Clinical Research Associate to join our team! As an In-House CRA here at Rho, you’ll have the opportunity to gain the necessary experience to grow into a traveling Clinical Research Associate (CRA) and work with the Project Manager, traveling CRAs and Lead CRA on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed. You’ll manage data entered into the CTMS (clinical trials management system) and other project tracking tools. You’ll also assist CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations. You may also have the opportunity to mentor other team members. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing: - Collect, track and review investigational site records relating to subject screening and enrollment - Assist in the development of study plans and status reports - Collect, track, and review all site regulatory documents - Assist with development and review of Informed Consent Forms - Interact with sites, clients, vendors and internal study team members - Maintain the clinical trials management system (CTMS) and other project tracking tools - Track study supplies and coordinate shipments of supplies to sites as needed - Manage the study Trial Master File (TMF) and ensure periodic TMF audits - Coordinate work with CRAs monitoring on-site - Perform on site co-monitoring and remote monitoring activities - Perform regular reviews of data entered by investigational site staff according to data review/monitoring guidelines