
Cancer Clinical Research Coordinator Associate - Bone Marrow Transplant (Hybrid)
Stanford, CA · HybridJobSeen 2w agoSeen in employer's feed today
Most applications go out cold — see where you stand first. No sign-up to start.
You apply on the employer's site, with no Olive account needed.
Watch jobs like this. New roles like this one near Stanford, CA, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Job overview
The Clinical Research Coordinator Associate supports the Bone Marrow Transplant clinical research program at the Stanford Cancer Institute, reporting to the BMT Clinical Research Manager. The role uses knowledge of the Institute’s mission and priorities to help ensure trial participant safety and well-being. The posting seeks candidates with strong interpersonal skills, attention to detail, professionalism, initiative, and flexibility.
Skills & qualifications
Skills
Qualifications
Full job description
Job Description
Cancer Clinical Research Coordinator Associate – BMT HYBRID
The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Clinical Research Coordinator Associate to help us enact our mission to reduce cancer mortality through comprehensive cancer research, treatment, education and outreach. Given the SCI's mission, breadth, and depth, it employs over 320 staff members in a fast-paced, team-oriented, and forward-thinking environment with tremendous opportunities for personal and professional growth. The Clinical Trial Office (CTO) is an integral component of the Stanford Cancer Institute. The vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting. You will be working with an unparalleled leading-edge community of faculty and staff who are fundamentally changing the world of health care in the cancer arena.
Reporting to the BMT Clinical Research Manager (CRM), the CRCA will be conversant in the goals, mission, and priorities of the Institute, and utilize this knowledge to ensure the safety and well-being of trial participants. We are seeking candidates with excellent interpersonal skills and attention to detail. Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative and flexibility.
DESIRED QUALIFICATIONS:
-
Knowledge of the principles of clinical research and federal regulations.
-
Familiarity with IRB guidelines and regulations.0
-
Previous experience with clinical research.
-
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
-
Strong oral and written communication skills
-
Excellent attention to detail
-
Proficiency in using computers, software, and web-based applications in a previous administrative setting
PHYSICAL REQUIREMENTS:*
-
Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
-
Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
-
Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
WORKING CONDITIONS:
Occasional evening and weekend hours.
WORK STANDARDS:
-
Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
-
Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
-
Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .
How this job compares
Set against the 641 open Clinical Research Coordinator jobs on Olive Jobs, counted November 7, 2026.
- Pay
- This postingNot listed
- US median$56–74K/yr162 salary ranges
- California median$38–44/hr25 hourly ranges
- Openings
- Olive Jobs lists 95 open Clinical Research Coordinator jobs in California and 641 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most in California
- Stanford University (this employer)36 open
- Cedars-Sinai15 open
- UCLA Health8 open
- Experience
- Clinical Research Coordinator postings that state a minimum ask for 2 years of experience at the median; the middle half ask for 1 to 3 years (420 postings).
- Education
- 191 of the 641 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 7, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
Prepare for this role
You've read the whole posting — now see how you match it.
