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

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in the USA. Main Responsibilities: - Act as Medical Monitor, performing comprehensive medical monitoring activities. - Respond to medical inquiries from investigational sites and trial teams. - Review patient eligibility and protocol deviations. - Oversee patient safety by reviewing medical data at patient and trial levels. - Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments. - Prepares scientific slides, attends and/or presents protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc. - Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams). - Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs). - Conducting medical training on selected trial-specific or non-trial-specific topics. Qualifications: - Medical Doctor degree required - Excellent knowledge and understanding of oncology and oncology clinical trials - At least 1 year of experience in medical monitoring in oncology trials - Current knowledge of ICH GCP guidelines - Advanced proficiency in MS Office in Word, Excel, and PowerPoint - Strong teamwork abilities and communication skills - Excellent level of English is required - Spanish language knowledge will be valued - Must be legally authorized to work in the country What TRIO Can Offer You: - Competitive Salary - 3 weeks of vacation plus paid Christmas Closure - 2 weeks paid personal/sick time - 100% health benefits for you and your family paid by TRIO - Flexible working hours - Monthly internet allowance - 401K Program 5% Salary Contribution - Home office allowance Pay Range: $110,000 - $150,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. Prior to applying please review TRIO's Applicant Information Notice To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation

Communicate with healthcare teams to clarify and obtain essential medical record documentation. Conduct in-depth chart reviews to ensure accurate coding and compliance with quality metrics, enhancing overall clinical documentation improvement efforts.

Monitor and manage clinical trials, ensuring compliance with protocols and regulatory requirements. Conduct site visits, verify data accuracy, and train site staff on procedures while maintaining effective communication with stakeholders.