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Clinical Research Coordinator 2

Stanford University

Redwood City, CAJobSeen todaySeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
Redwood City, CA
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Emmanuel Mignot Lab at Stanford University seeks a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively complex projects. The coordinator independently manages significant aspects of a large study or all aspects of one or more small studies. Desired qualifications include sleep medicine clinical-trial experience, FDA audit participation, study start-up and close-out, patient recruitment and retention, and experience with EDC systems and ECGs.

Skills & qualifications

RequiredNice to have

Skills

Clinical Trial Start-UpClinical Trial Close-OutFDA Audit SupportInvestigator Site FilesClinical Trial DocumentationRegulatory ComplianceSleep MedicineClinical Research Staff SupervisionPatient RecruitmentPatient RetentionElectronic Data CaptureVendor PortalsECGStandingWalkingTwistingBendingStoopingSquattingFine GraspingLiftingCarryingPushingPullingKneelingCrawlingClimbing LaddersForceful Grasping

Qualifications

3+ Years Sleep Medicine Clinical TrialsStudy Lead for FDA-Audited TrialFDA Audit ParticipationTraining Four+ Clinical Research Assistants

Full job description

Job Description

The Emmanuel Mignot Lab at Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies.

DESIRED QUALIFICATIONS:

  • 3+ years of experience working in Sleep Medicine clinical trials.

  • Experience with clinical trial study start-up and close-out activities.

  • Previous experience serving as a study lead for a clinical trial that underwent an FDA audit.

  • Direct participation and experience supporting an FDA audit.

  • Strong knowledge and experience maintaining Investigator Site Files (ISF) and ensuring proper documentation and organization.

  • Strong understanding of clinical trial documentation, regulatory requirements, and study compliance.

  • Knowledge of sleep medicine disorders

  • Experience participating in FDA audits

  • Experience training and supervising a group of at least four Clinical Research Assistants (CRCAs)

  • Experience participating in study start-up and closeout activities

  • Experience recruiting and retaining complex patient populations in clinical trials

  • Experience using Electronic Data Capture (EDC) systems and vendor portals

  • Experience performing ECGs

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:

  • Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.

  • May require extended or unusual work hours based on research requirements and business needs.

How this job compares

Set against the 607 open Clinical Research Coordinator jobs on Olive Jobs, counted November 4, 2026.

Pay
  • This postingNot listed
  • US median$57–74K/yr153 salary ranges
  • US median$24–36/hr179 hourly ranges
Openings
Olive Jobs lists 68 open Clinical Research Coordinator jobs in California and 607 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most in California
Experience
This posting asks for at least 3 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (397 postings).
Education
191 of the 607 open Clinical Research Coordinator jobs (31%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 4, 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.

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