Top 33 clinical research coordinator Jobs in folsom ca

Clinical Research & Trial Development Coordinator
Verity MD —Folsom, CA
- $28 - $38 an hour
- Part-time
- Google Workspace
- HIPAA
- Mid-level
- Relocation assistance
Quick Apply
6d
Clinical Support Coordinator
Mercy San Juan Medical Center —Carmichael, CA
- $30.91 - $45.98 an hour
- Full-time
- Acute care
- Hospital
- Research
Clinical Research Coordinator II
Shriners Children's —Sacramento, CA
- $32.40 - $48.60 an hour
- Full-time
- Hospital
- Mid-level
- 3 years
Quick Apply
Clinical Research Coordinator
Nor Cal Clinical Research —Rocklin, CA
- $20 - $30 an hour
- Full-time
- Mid-level
- Clinic
- Pediatrics
- Paid holidays
- Health insurance
Quick Apply
8d
Clinical Research Coordinator- Greenback
Retina Sacramento MSO LLC —Sacramento, CA
- $31.00 - $44.50 an hour
- Full-time
- Private practice
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Clinical Research Assistant- Parkcenter
Retina Sacramento MSO LLC —Sacramento, CA
- $26.50 - $33.50 an hour
- Full-time
- Private practice
- Anatomy knowledge
- High school diploma or GED
- Paid holidays
- Health insurance
8d
Clinical Research Associate II - FSP
Precision Medicine Group —Sacramento, CA
- $91,500 - $137,300 a year
- Online Application
- Remote
- Word processing
- Mid-level
- Master's degree
13d
Clinical Research Coordinator
Integrative Skin Science Research —Sacramento, CA
- $20 - $30 an hour
- Full-time
- Mid-level
- Clinic
- Pediatrics
- Paid holidays
- Health insurance
Quick Apply
8d
Program Services Clinical Coordinator
Mentor Community Services —Rancho Cordova, CA
- $47,964.80 a year
- Full-time
- CPR Certification
- Mid-level
- Driver's License
- Paid holidays
- Paid time off
Weekend Clinical Intake Coordinator (LVN / RN)
21st Century Home Health Services Inc. —Sacramento, CA
- Choose your own hours
- Clean driving record
- LVN
- RN License
- Opportunities for advancement
- Flexible schedule
Quick Apply
Weights and Research Coordinator
R+L Carriers —West Sacramento, CA
- $70,305 a year
- Full-time
- Computer literacy
- Analysis skills
- Fair chance
- Paid holidays
- Health insurance
1d
Family Research Project Coordinator
NorCal —Sacramento, CA
- $74,970 - $78,719 a year
- Email
- Writing skills
- Mid-level
- Bachelor's degree
2d
Clinical Onboarding & Compliance Coordinator
Sacramento Ultrasound Institute —Sacramento, CA
- $20 - $24 an hour
- Full-time
- CPR Certification
- OSHA
- BLS Certification
Quick Apply
Clinical Coordinator - Neuro Rehab
Rehab Without Walls Neuro Rehabilitation —Sacramento, CA
- $45 - $50 an hour
- Full-time
- CPR Certification
- Nursing
- RN License
11d
Practicum Coordinator, M.A. in Counseling Psychology (MACP), Full-Time Clinical Faculty
William Jessup University (4-year Christian University) —Rocklin, CA
- $65,000 - $75,000 a year
- Full-time
- Hybrid work
- LMFT
- Ability to walk for extended periods
- Licensed Clinical Social Worker
- Health insurance
- Dental insurance
Quick Apply
Clinical Program Coordinator (Cut Hypertension)
Roots Community Health Center —Sacramento, CA
- $24.04 - $26.04 an hour
- Full-time
- Primary Care
- Mid-level
- Data entry
Quick Apply
Ultrasound Technology Program Clinical Coordinator
Distro —Sacramento, CA
- $105,000 - $125,000 a year
- Full-time
- Laboratory
- Classroom
- Bachelor of Science
- Health savings account
- Disability insurance
Quick Apply
Radiographic Imaging Clinical Coordinator – Full-time
Gurnick Academy of Medical Arts —Sacramento, CA
- $110,000 - $120,000 a year
- Full-time
- School experience
- Bachelor of Science
- Physical & Rehabilitation Medicine
- Health savings account
- Disability insurance
Radiographic Imaging Clinical Coordinator
Distro —Sacramento, CA
- $110,000 - $120,000 a year
- Full-time
- School experience
- Management
- Bachelor of Science
- Health savings account
- Disability insurance
Quick Apply
13d
Clinical Screening Coordinator - Roseville, CA
Gainwell Technologies —Roseville, CA
- $32,600 - $46,500 a year
- Full-time
- Customer service
- Mid-level
- Communication skills
- Travel reimbursement
- Profit sharing

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Clinical Research & Trial Development Coordinator

Verity MD
Folsom, CA

Quick Apply

Job Details

Part-time | Contract
$28 - $38 an hour
6 days ago

Benefits

Relocation assistance

Qualifications

Professional ethics
Healthcare Administration
Bachelor's degree
Public Health
Health Science
Project task coordination
Organizational skills
Clinical confidentiality policies

Full Job Description

About VerityMD Neurology

VerityMD Neurology is a growing outpatient neurology practice serving patients in the Sacramento, Carmichael, and Folsom region. We are focused on timely access, high-quality neurologic care, diagnostic services, innovation, and future research opportunities for patients with neurologic conditions.

Position Summary

VerityMD Neurology is seeking a part-time Clinical Research & Trial Development Coordinator to help build the foundation for a future clinical trials program.

VerityMD is not currently running active clinical trials. This role will initially focus on helping the practice become clinical-trial-ready through sponsor outreach, clinical trial opportunity tracking, feasibility preparation, site profile development, patient registry planning, and basic research workflow setup.

This is a good opportunity for someone with clinical research experience who is organized, proactive, and able to help a growing neurology practice develop a research program from the ground up. The role may expand over time if VerityMD secures active clinical trials.

Expected Hours

This is a part-time/project-based role expected to start at approximately 10–15 hours per week.

During the initial 4–6 weeks, the coordinator will focus on building VerityMD’s clinical research foundation, including sponsor outreach, clinical trial opportunity tracking, feasibility preparation, site profile development, and basic research workflow templates.

After the initial setup period, hours may adjust based on workload:

5–10 hours per week if the role is primarily maintaining outreach and tracking opportunities.

15–20 hours per week if sponsor discussions, feasibility questionnaires, site qualification calls, or research program development activities increase.

20–30 hours per week may be considered if VerityMD moves toward active trial start-up.

The role may grow into a full-time Clinical Trial Coordinator position once VerityMD has active clinical trials requiring regular patient screening, visit coordination, regulatory documentation, data entry, and sponsor communication.

Key Responsibilities

Research Program Development

Assist in building a clinical research roadmap for VerityMD Neurology.

Identify potential clinical trial opportunities relevant to outpatient neurology, including Alzheimer’s disease, mild cognitive impairment, migraine, Parkinson’s disease, multiple sclerosis, epilepsy, neuropathy, stroke, and neurodiagnostic studies.

Identify and track potential sponsors, contract research organizations, academic partners, and industry-sponsored research opportunities.

Maintain a clinical trial opportunity tracker with study name, sponsor, disease area, eligibility, contact information, feasibility status, and next steps.

Assist leadership in determining which research opportunities are clinically appropriate, operationally feasible, and financially sustainable.

Trial Readiness and Infrastructure

Help prepare VerityMD to become a study site for industry-sponsored, registry-based, and observational studies.

Create a VerityMD clinical research site profile summarizing provider expertise, clinic capabilities, patient population, diagnostic services, location, and operational strengths.

Assist with preparing site feasibility questionnaires and capability surveys.

Organize commonly requested research documents, including provider CVs, licenses, training certificates, site information, lab/imaging capabilities, and clinic profiles.

Create templates for screening logs, delegation logs, training logs, regulatory binders, patient tracking sheets, and visit checklists.

Help develop basic standard operating procedures for research intake, patient screening, informed consent workflow, documentation, and sponsor communication.

Patient Registry and Recruitment Preparation

Help create condition-specific patient registries for possible future studies.

Work with leadership to identify high-value research areas based on VerityMD’s patient population.

Support development of patient-friendly research interest forms and education materials.

Assist with pre-screening workflows once appropriate studies become available.

Maintain careful documentation while following privacy and HIPAA requirements.

Sponsor and Partner Communication

Serve as an administrative contact for potential research sponsors and contract research organizations.

Help coordinate introductory calls, feasibility discussions, and site qualification steps.

Prepare summary materials describing VerityMD’s clinical services, provider expertise, diagnostic capabilities, and patient access.

Maintain organized follow-up with sponsors and research partners.

Provide leadership with regular updates on research leads, pending tasks, barriers, and next steps.

Future Responsibilities if Trials Become Active

If active trials are secured, the role may expand to include:

Coordinating patient research visits.

Maintaining regulatory binders and study documents.

Entering data into electronic data capture systems.

Supporting informed consent workflows under investigator supervision.

Tracking adverse events, serious adverse events, and protocol deviations under investigator guidance.

Coordinating monitor visits.

Managing study calendars and patient follow-up.

Supporting audit-ready documentation.

Qualifications

Bachelor’s degree preferred in health sciences, public health, biology, neuroscience, psychology, healthcare administration, or a related field.

Prior clinical research or clinical trial coordination experience preferred.

Experience with neurology, Alzheimer’s disease, mild cognitive impairment, migraine, epilepsy, Parkinson’s disease, multiple sclerosis, stroke, or neuropathy research is a plus.

Familiarity with Good Clinical Practice, HIPAA, Institutional Review Board workflows, informed consent, and clinical trial documentation preferred.

Comfortable with spreadsheets, Google Workspace, Microsoft Office, electronic medical records, and online sponsor portals.

Clinical Research Coordinator certification is preferred but not required.

Required Skills

Highly organized and detail-oriented.

Able to work independently with minimal supervision.

Strong written and verbal communication skills.

Comfortable contacting sponsors, vendors, and research partners.

Able to build workflows from scratch.

Strong follow-through and task tracking.

Comfortable working in a growing outpatient neurology practice.

Professional, ethical, and careful with patient confidentiality.

Key Performance Goals for the First 90 Days

Create a clinical research opportunity tracker.

Identify and contact potential neurology trial sponsors and contract research organizations.

Prepare a VerityMD clinical research site profile.

Develop a clinical trial readiness checklist.

Create basic research workflow templates.

Build an initial list of high-priority neurologic disease areas for potential trials.

Support leadership in deciding which trial opportunities are operationally and financially appropriate.

Provide regular updates on outreach progress, sponsor responses, and next steps.

Compensation

The pay range is $28–$38 per hour, depending on experience.

Candidates with prior clinical trial coordination experience, neurology research experience, sponsor or contract research organization communication experience, or the ability to independently prepare a practice for trial readiness may be considered at the higher end of the range.

Growth Opportunity

This position has the potential to grow into a larger role if VerityMD secures active clinical trials and develops a sustainable research program. Full-time status may be considered in the future if active studies require regular patient screening, visit coordination, regulatory documentation, data entry, and sponsor communication.

Pay: $28.00 - $38.00 per hour

Benefits:

Relocation assistance

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in folsom ca

Clinical Research & Trial Development Coordinator

Clinical Support Coordinator

Clinical Research Coordinator II

Clinical Research Coordinator

Clinical Research Coordinator- Greenback

Clinical Research Assistant- Parkcenter

Clinical Research Associate II - FSP

Clinical Research Coordinator

Program Services Clinical Coordinator

Weekend Clinical Intake Coordinator (LVN / RN)

Weights and Research Coordinator

Family Research Project Coordinator

Clinical Onboarding & Compliance Coordinator

Clinical Coordinator - Neuro Rehab

Practicum Coordinator, M.A. in Counseling Psychology (MACP), Full-Time Clinical Faculty

Clinical Program Coordinator (Cut Hypertension)

Ultrasound Technology Program Clinical Coordinator

Radiographic Imaging Clinical Coordinator – Full-time

Radiographic Imaging Clinical Coordinator

Clinical Screening Coordinator - Roseville, CA

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