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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Showing 5 of 784+ Clinical Research Coordinator jobs
Job Summary:
Under the supervision of a Clinical Research Supervisor, Clinical Research Manager, and/or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey-level work at the next level within the series.
May be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned.
Department Overview:
The Cutaneous Oncology research group focuses on clinical trials aimed at the treatment of advanced skin cancers, especially melanoma. Melanoma is the deadliest skin cancer, one of the most common cancers, and one of the few cancer types with increasing incidence. Current research in progress includes immunotherapies, targeted therapies, mRNA, viral vectors, and other intralesionally injected drugs as well as some exploratory research involving tumor tissue and blood products.
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is one of only two cancer centers in the Bay Area to receive the prestigious designation of “comprehensive” from the National Cancer Institute (NCI).
The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer. The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.
Required Qualifications:
- HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
- Attention to details.
- Proficiency with Microsoft Word, PowerPoint, and Windows.
- Excellent analytical and problem-solving skills.
- Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
- Ability to establish cooperative working relationships with patients, co-workers, & physicians.
Preferred Qualifications:
- Demonstrated proficiency with medical terminology.
- Experience working with patients or study subjects.
- Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.
Job Summary:
Under the supervision of a Clinical Research Supervisor, Clinical Research Manager, and/or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey-level work at the next level within the series.
May be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned.
Department Overview:
The Cutaneous Oncology research group focuses on clinical trials aimed at the treatment of advanced skin cancers, especially melanoma. Melanoma is the deadliest skin cancer, one of the most common cancers, and one of the few cancer types with increasing incidence. Current research in progress includes immunotherapies, targeted therapies, mRNA, viral vectors, and other intralesionally injected drugs as well as some exploratory research involving tumor tissue and blood products.
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is one of only two cancer centers in the Bay Area to receive the prestigious designation of “comprehensive” from the National Cancer Institute (NCI).
The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer. The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.
Required Qualifications:
- HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
- Attention to details.
- Proficiency with Microsoft Word, PowerPoint, and Windows.
- Excellent analytical and problem-solving skills.
- Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
- Ability to establish cooperative working relationships with patients, co-workers, & physicians.
Preferred Qualifications:
- Demonstrated proficiency with medical terminology.
- Experience working with patients or study subjects.
- Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.
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Find JobsClinical Research Coordinator Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Medpace59
- University of California - San Francisco48
- Emory University32
- University of Pennsylvania29
- Dana-Farber Cancer Institute27
Top Industries Hiring
- Education377
- Healthcare & Medical Services311
- Biotechnology & Pharmaceuticals69
- Science & Research60
- Consulting & Professional Services18
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 Medpace, University of California - San Francisco, and Emory University, with the largest share of openings in California, Massachusetts, and Ohio, based on current listings on Migrate Mate as of June 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 11% of clinical research coordinator openings are fully remote or hybrid as of June 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.
See All 784+ Clinical Research Coordinator Jobs
Jump back to the full list of openings and apply to any clinical research coordinator role that fits.
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