Job detail

Clinical Research Coordinator (Carlsbad, CA)

Profound Research

#Vital Signs #Vendor Management #Regulatory Compliance #Patient Care #Site Operations #Blood Draws #Data Management #EKG #Clinical Assessments

Quick overview

The Clinical Research Coordinator manages all clinical trial activities in compliance with study protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical research operations.

Requirements summary

Candidates must have a degree (Bachelor's, Associate's, or High School with relevant experience) and at least 2 years of experience in the life science industry. Additionally, 1 year of specific Clinical Research Coordinator experience and the ability to perform clinical assessments like blood draws and EKGs are required.

high schoolassociate degreebachelor degreeCommunicationEKGsRegulatory complianceData collectionVendor managementVital signsBlood drawsSpecimen processingClinical assessmentsAdverse event reportingClinical trial managementSubject recruitmentIATA certificationProtocol trainingSource document reviewICH-GCP certification

Job description

About profound research

Profound 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 Options

Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research

Our 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 Do
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

Clinical Research Coordinator (Carlsbad, CA)

Quick overview

Requirements summary

Job description

About profound research

Our Values

Benefits

What We’re Looking For

WHY JOIN PROFOUND RESEARCH? • Meaningful Impact

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