Contractor- Assistant Clinical Research Coordinator (Oceanside, CA)

Profound Research • Oceanside, CA

2d • Onsite

About The Position

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.

If you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research. 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 high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.

This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.

Requirements

• 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
• Strong attention to detail and ability to follow structured processes accurately
• Clear, professional communication with patients, caregivers, clinical staff, and internal team members
• Proficient with standard computer tools; able to learn new systems quickly
• Familiarity with medical terminology and basic clinical procedures
• Ability to maintain professionalism, confidentiality, and care when working with patients and sensitive information

Nice To Haves

• Prior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
• Experience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
• Experience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
• Prior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
• Experience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems

Responsibilities

• Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
• Assist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
• Perform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
• Help prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
• Interact directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
• Work closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
• Follow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
• Help maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
• Communicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
• Contribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter

Benefits

• Competitive compensation
• health insurance
• PTO
• retirement plan
• professional development support

What This Job Offers

• Career Level: Entry Level
• Education Level: High school or GED