Contractor- Assistant Clinical Research Coordinator (San Diego)

Profound Research; Sacramento (CA); On-site; USD 42,000 - 66,000; Part time

Benefits offered by this job

Health insurance

PTO

Retirement plan

Professional development support

Competitive compensation

Job summary

Profound Research is seeking an Assistant Clinical Research Coordinator to support high-volume vaccine studies at a site-based facility. You’ll gain hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced environment.

You’ll work under experienced staff, learning to apply GCP standards and site procedures. This 1099 role offers growth potential toward full-time opportunities based on performance and business needs.

Qualifications

• Essential qualifications include a high school diploma or technical degree with 3+ years of life sciences experience, or an Associate’s/Bachelor’s with relevant experience.
• Excellent attention to detail and ability to follow structured processes.
• Clear, professional communication with patients, caregivers, staff, and internal teams.
• Proficiency with standard computer tools; ability to learn new systems quickly.
• Familiarity with medical terminology and basic clinical procedures.
• Ability to maintain professionalism and confidentiality with patients and sensitive information.

Responsibilities

• Coordinate high-volume vaccine clinical trials, including patient visits, scheduling, and study procedures.
• Assist with data collection and documentation while applying Good Clinical Practice standards.
• Perform clinical procedures such as vital signs, phlebotomy, and specimen processing as trained.
• Prepare for and support efficient participant visits, rooming patients, organizing supplies, and keeping the site team aligned.
• Interact with study participants, explain visit steps, answer questions, and ensure patient comfort.
• Collaborate with CRCs and site leadership, seek feedback, and build clinical research knowledge.
• Follow study protocols, SOPs, GCP, GDP, and infection control to ensure compliant, audit-ready trial execution.
• Maintain organized study materials, supplies, documentation, and lab workflows for visits and site operations.
• Communicate clearly with site team about patient needs, visit flow, and documentation status.
• Contribute to a fast-paced, team-based site environment where quality, urgency, and patient experience matter.

Skills

Attention to detail

Clear communication

Professionalism

Ability to learn new systems

Medical terminology familiarity

Team-based collaboration

Education

High school diploma or technical degree with 3+ years life sciences experience

Associate’s degree with 1+ year life sciences experience

Bachelor’s degree with relevant coursework/experience

Job description

Job Description

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.

Why This Role Exists

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 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.

What You’ll Do

• 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

What We’re Looking For

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. The rest we’ll help you build.

Essential Qualifications

• 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

Preferred Qualifications

• 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

Engagement Details

This is a 1099 independent contractor opportunity designed to support current high‑volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full‑time employment over time.

Physical Requirements & Work Environment

• 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
• 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

Why 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 matters

Professional Growth:

We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career

Leadership & 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 time

Collaborative Culture:

You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well

Full Benefits Package:

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

Diverse Clinical Exposure:

• Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.