Clinical Research Assistant: Patient-Focused Trials

About Profound Research Profound Research partners with community physicians to offer clinical trials as a therapeuticoptionfor their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies whilemaintainingthe trusted patient-physician relationship. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritizethe patient-physicianrelationship, ensuring every interaction is service-oriented and patient-centered. Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues. Solution Orientation: We embrace challenges with a positive mindset, communicate directly, andidentifyand implement effective solutions with efficiency. Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards. Start Your Career in Clinical Research Ifyou’recurious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins. As an Assistant Clinical Research Coordinator at Profound Research,you’llwork alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies theycouldn’totherwise reach.You’lllearn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time. Thisisn’ta behind-the-desk role.You’llbe present with patients, part of a team, and contributing to research that has real-world impact from day one. WhatYou’llDo Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures Assistwith data collection and documentation, learning to apply the rigorous standards that clinical research demands Perform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing Interact directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process Work closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base Contribute to a compliant, audit-readysite by following established protocols, SOPs, and Good Documentation Practices WhatWe’reLooking For Youdon’tneed to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about thepatientexperience. The restwe’llhelp you build. High school diploma or technical degree with 3+ years of relevantexperience in life sciences, ORAssociate’sdegree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting Familiarity with medical terminology and basic clinical procedures is a plus Comfortable working in a fast-paced, team-based environment Proficient with standard computer tools; able to learn new systems quickly ICH-GCP and IATA certificationrequiredwithin a definedtimeframeupon hire (we’llsupport you through it) Physical Requirements & Work Environment This role is performedon-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed May be required to wear personal protective equipment (PPE) in accordance with facility protocols Travel between company sites, meetings, or partner locations may be required Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role Why Join Profound Research? Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time Collaborative Culture: You’llwork alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization #J-18808-Ljbffr Profoundresearch