This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
Assistant Clinical Research CoordinatorProfound 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.Start Your Career in Clinical ResearchIf you're curious 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'll work 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 they couldn't otherwise reach. You'll learn 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.This isn't a behind-the-desk role. You'll be present with patients, part of a team, and contributing to research that has real-world impact from day one.What You'll DoSupport the coordination of active clinical trials, including patient visits, scheduling, and study-related proceduresAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demandsPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processingInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the processWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge baseContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation PracticesWhat We're Looking ForYou don't need 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 the patient experience. The rest we'll help you build.High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate's degree with 1+ year of relevant experience, OR Bachelor's degree with relevant coursework or experience in a clinical or life sciences settingFamiliarity with medical terminology and basic clinical procedures is a plusComfortable working in a fast-paced, team-based environmentProficient with standard computer tools; able to learn new systems quicklyICH-GCP and IATA certification required within a defined timeframe upon hire (we'll support you through it)Physical 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
Worksite address
carlsbad, CA, 92011, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.