Clinical Research Coordinator- Internal Med (Oceanside, CA)

Benefits

Qualifications

• •You’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 experience
• •Experience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
• •Comfortable working independently and managing competing priorities
• •Strong documentation skills and familiarity with EDC platforms and clinical trial management systems
• •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
• •7 more items(s)

Responsibilities

• •We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues
• •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
• •Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
• •Execute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
• •Lead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
• •Maintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
• •Track and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
• •Communicate directly and professionally with investigators, sponsors, CROs, and internal teams
• •Support site readiness for monitoring visits and audits
• •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
• •11 more items(s)