Clinical Research Coordinator

Clinical Research Coordinator IProfound Research partners with community physicians to offer clinical trials as a therapeutic option for 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 while maintaining the trusted patient-physician relationship.Our Mission: Improving Lives by Providing Advanced Therapeutic OptionsOur Vision: Creating the Absolute Best Patient-Physician Experience in Clinical ResearchOur Values:Compassion: We prioritize the patient-physician relationship, 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, and identify and 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.Own Your Studies. Grow Your Career.If you're ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.As a Clinical Research Coordinator I at Profound Research, you'll serve as the primary coordinator for assigned studies at one of our sites. You'll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn't a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.What You'll DoServe as primary coordinator for assigned clinical trials, managing study activities from start-up through closeoutExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentationLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experienceMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systemsTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirementsCommunicate directly and professionally with investigators, sponsors, CROs, and internal teamsSupport site readiness for monitoring visits and auditsWhat We're Looking ForYou've got some experience in clinical research and you're ready for more responsibility. You're organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.Bachelor's degree with 1+ year of relevant experience, OR Associate's degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experienceExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processingComfortable working independently and managing competing prioritiesStrong documentation skills and familiarity with EDC platforms and clinical trial management systemsPhysical Requirements & Work EnvironmentThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environmentRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materialsMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as neededMay be required to wear personal protective equipment (PPE) in accordance with facility protocolsTravel between company sites, meetings, or partner locations may be requiredReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the roleWhy 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 mattersProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your careerLeadership & 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 timeCollaborative Culture: You'll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it wellFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development supportDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that's rare in a single organization