Assistant Clinical Research Coordinator- Internal Medicine (Oceanside, CA)

Benefits

Qualifications

• •You 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
• •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 setting
• •Comfortable working in a fast-paced, team-based environment
• •Proficient with standard computer tools; able to learn new systems quickly
• •ICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
• •This role is performed on-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
• •6 more items(s)

Responsibilities

• •We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues
• •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
• •You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one
• •Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
• •Assist with 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-ready site by following established protocols, SOPs, and Good Documentation Practices
• •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
• •9 more items(s)