Clinical Research Coordinator Jobs
Clinical Research Coordinator jobs are open across academic medical centers, pharmaceutical companies, contract research organizations, and hospitals, at every level from entry-level to senior and lead, with specializations in oncology trials, device studies, and Phase I-IV clinical operations. Find a role that fits from the openings below and apply directly.
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Job Title: Clinical Research Coordinator (CRC I / CRC II) Location: Los Angeles, CA (On-Site) Employment Type: W-2, Full-Time (or Part-Time transitioning to Full-Time) Schedule: Monday - Friday, standard clinic hours (No evenings or weekends) Start Date: Immediate / ASAP Compensation: $25.00 - $35.00 / hour (commensurate with experience)
Position Overview We are seeking a detail-oriented, proactive Clinical Research Coordinator (Entry-Level / CRC I or CRC II) to join our growing clinical research site in Los Angeles, California. In this role, you will manage the day-to-day clinical and administrative operations of assigned clinical trials under the supervision of the Principal Investigator (PI) and Site Leadership. This is an ideal opportunity for a coordinator with a strong foundation in clinical trials who wants to grow their career in a supportive, weekday-only clinic environment.
Key Responsibilities
- Study Execution & Protocol Compliance: Coordinate clinical trial activities from startup through closeout in strict accordance with study protocols, Good Clinical Practice (GCP), ICH guidelines, and FDA regulations.
- Patient Recruitment & Screening: Prescreen clinic schedules and patient charts, conduct recruitment outreach, explain study procedures to prospective participants, and facilitate the Informed Consent process alongside the PI.
- Study Visits & Procedures: Conduct scheduled participant visits, obtain vital signs, collect medical histories, administer questionnaires, and perform or coordinate specimen collection, processing, and shipping (IATA).
- Data Management: Accurately record source documentation and enter timely clinical data into Electronic Data Capture (EDC) systems; resolve data queries within sponsor timelines.
- Sponsor & Monitor Coordination: Prepare for and host Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and closeout visits; serve as a primary point of contact for Clinical Research Associates (CRAs) and sponsors.
- Safety & Regulatory Support: Track and report Adverse Events (AEs) and Serious Adverse Events (SAEs) promptly to the PI, sponsor, and IRB; assist with maintaining Investigator Site Files (ISF) and regulatory binders.
- Investigational Product (IP) Accountability: Receive, store, dispense, and maintain accurate accountability logs for study drug or device supplies as delegated.
Qualifications & Requirements
- Experience: Minimum of 2 to 3 years of hands-on experience working as a Clinical Research Coordinator or in direct clinical trial operations (open to multi-specialty backgrounds; no specific therapeutic area required).
- Knowledge Base: Solid working understanding of ICH-GCP guidelines, regulatory documentation, source documentation standards, and general EDC/EMR navigation.
- Soft Skills: Exceptional organizational skills, strong attention to detail, clear communication with patients and physicians, and the ability to manage multiple protocols simultaneously.
- Work Authorization: Must be authorized to work in the United States as a W-2 employee, able to commute reliably to Los Angeles, CA, and available to start immediately.
Preferred Qualifications (Nice-to-Haves)
- California CPT-1 Phlebotomy Certification or hands-on blood draw and lab processing experience.
- ACRP (CCRC) or SOCRA (CCRP) certification.
- Current GCP and IATA certifications (or willingness to complete upon hire).
Compensation & Benefits
- Hourly Pay: $25.00 - $35.00 / hour, based on coordinator level and certifications.
- Comprehensive Benefits Package (Full-Time):
- Medical, Dental, and Vision insurance
- 401(k) retirement plan
- Paid Time Off (PTO) and paid holidays
- Work-Life Balance: Predictable Monday through Friday daytime schedule with no evening or weekend shifts.
How to Apply Please submit your updated resume along with your target hourly rate and earliest available start date.
Pay: $25.00 - $35.00 per hour
Expected hours: 20.0 – 40.0 per week
Benefits:
- 401(k)
- Dental insurance
- Paid time off
Work Location: In person
Clinical Research Coordinator Jobs by Experience Level
Top Cities Hiring Clinical Research Coordinators
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Find JobsClinical Research Coordinator Job Market
Who's Hiring
- Washington University in St. Louis33
- Iterative Health24
- Johns Hopkins University19
- Emory University17
- Medical College of Wisconsin16
Top Industries Hiring
- Education53
- Healthcare & Medical Services46
- Biotechnology & Pharmaceuticals13
- Consulting & Professional Services6
- Science & Research2
What Employers Look For
The qualifications that appear most often in clinical research coordinator jobs.
- Bachelor's degree in a life science, nursing, or health-related field
- Prior experience coordinating clinical trials under ICH-GCP guidelines
- Proficiency with electronic data capture systems such as REDCap, Medidata Rave, or Veeva Vault
- CCRP or CCRC certification preferred or required at senior levels
- Demonstrated ability to obtain informed consent and maintain regulatory binders
- Familiarity with FDA regulations governing human subjects research and study sponsor requirements
Tips for Your Clinical Research Coordinator Job Search
Tailor your resume to protocol experience
List the specific therapeutic areas, trial phases, and patient populations you've worked with. Hiring managers scan for oncology, CNS, or cardiology experience before reading further, so burying protocol details in a general summary costs you interviews.
Earn your CCRP before applying broadly
The Certified Clinical Research Professional credential signals you meet national competency standards. Many postings list it as preferred rather than required, but candidates who hold it consistently move faster through applicant screening at larger research sites.
Apply early to roles that fit
Migrate Mate lists clinical research coordinator openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Filter openings by phase and sponsor type
Industry-sponsored Phase III trials at CROs reward speed and volume, while investigator-initiated studies at academic centers reward protocol design experience. Knowing which environment suits you lets you target postings where your strengths are actually valued.
Prepare a protocol deviation walkthrough
Interviewers for coordinator roles almost always ask how you handled a protocol deviation or an adverse event. Prepare a concise, factual narrative that covers what happened, what you documented, who you notified, and how the site resolved it.
Negotiate start date around IRB timelines
If you're mid-study at your current site, flag that in your offer conversation. Research coordinators who can name a realistic handoff date and document open queries before leaving are far better positioned to negotiate a later start without losing the offer.
Clinical Research Coordinator Jobs: Frequently Asked Questions
Which companies are hiring the most clinical research coordinators?
The companies hiring the most clinical research coordinators right now include Washington University in St. Louis, Iterative Health, and Johns Hopkins University, with the largest share of openings in California, Florida, and Texas, based on current listings on Migrate Mate as of November 2026. Academic health systems and large CROs consistently account for the majority of open positions nationwide.
How many clinical research coordinator jobs are remote?
About 30% of clinical research coordinator openings are fully remote or hybrid as of November 2026, though most hands-on patient-facing roles require on-site presence. Regulatory affairs support, data coordination, and sponsor-facing study management roles are the sub-areas most likely to offer remote or hybrid flexibility.
How do you become a clinical research coordinator?
Start with a bachelor's degree in a life science, nursing, or public health field, then complete a GCP training certification, which most sites require before you can work with study participants. Gain initial exposure through a clinical research assistant or data coordinator role, build hands-on protocol experience, and pursue your CCRP once you meet the eligibility hours to advance to a full coordinator position.
Can you get a clinical research coordinator job with little or no experience?
Yes, entry-level coordinator roles exist specifically for candidates with a relevant degree but limited trial experience. Target academic medical centers and community research sites, which are more likely to train new coordinators than large CROs. Volunteering on an IRB, completing a clinical research certificate program, or shadowing an existing coordinator strengthens your application before your first paid role.
What does the clinical research coordinator interview process look like?
Most sites run a phone screen with HR followed by a panel interview with the principal investigator and a senior coordinator. Expect scenario questions on informed consent, protocol deviations, and adverse event reporting. Some sponsors add a practical exercise, such as reviewing a mock protocol excerpt or working through an eligibility checklist, before extending an offer.
Where can I find and apply to clinical research coordinator jobs?
You can find and apply to clinical research coordinator jobs on Migrate Mate, which lists current openings from across the United States. Search the listings to find roles that match your therapeutic area, site type, and experience level, then apply directly to each position that fits.
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