Clinical Research Coordinator 2 (Fixed-term 2 years)

Stanfordlivetickets; Palo Alto (CA); Hybrid; USD 85,000 - 97,000; Full time

Benefits offered by this job

Health benefits

Flexible work options

Tuition assistance

PTO 18+ days

Commuter benefits

Job summary

Stanford University’s School of Medicine invites applications for a Clinical Research Coordinator 2 (CRC2) on a fixed-term 2-year appointment. The role spans multiple complex industry-sponsored trials in ICU and OR settings, with long-term outpatient follow-up and enrollment across adult patient populations.

You will lead recruitment, manage study data, collaborate with nurses, pharmacy staff, and principal investigators, ensure regulatory compliance, and support budget tracking and regulatory

Qualifications

• Bachelor's degree in a related field and a minimum of two years of clinical research experience or an equivalent combination of education and relevant experience.
• Experience coordinating complex industry-sponsored clinical trials in critical care and OR settings.
• Knowledge of HIPAA and FDA regulatory requirements and good clinical practices.

Responsibilities

• Lead subject recruitment and enrollment goals for multiple trials.
• Oversee data management: organize, collect, report, monitor data; extract and interpret results.
• Collaborate on project schedules, targets, and accountability; assist with performance evaluations.
• Train or mentor new staff or students; assist with hiring and evaluations.
• Audit operations to ensure regulatory compliance; monitor IRB submissions and respond to queries.
• Monitor adverse events and communicate with investigators and sponsors; resolve study queries.

Skills

Clinical trial coordination

EMR systems experience

Informed consent in hospital setting

Education

Bachelor's degree in related field

Tools

Microsoft Office

Database applications

Job description

Clinical Research Coordinator 2 (Fixed-term 2 years)

Stanford, CA, United States (Hybrid)

Job Description

The Department of Anesthesiology, Perioperative, and Pain Medicine, at Stanford University’s School of Medicine, is a world-leading department that offers comprehensive training and perioperative patient care, pain management, and critical care medicine as well as cutting‑edge research, encompassing a wide spectrum of programs in basic, translational, clinical, health services and medical education.

The Department of Anesthesiology, Perioperative, and Pain Medicine is in search of a Clinical Research Coordinator 2 (CRC2) – Fixed-term 2 years to coordinate a dynamic portfolio of multiple complex clinical trials in various stages of the study life‑cycle, from start‑up through closeout. Participant populations are primarily adult patients in critical care and operative spaces, and will require long‑term outpatient follow‑up. Evolving study portfolio is primarily industry‑sponsored and includes research on treatments for Sepsis, Acute Respiratory Distress Syndrome, and Acute Kidney Injury. The CRC2 will participate in the identification, recruitment, and enrollment of participants. Trial design will sometimes require unusual work hours, including nights and weekends. The CRC2 will collaborate with other team members to collect key study measures, maintaining the integrity of critical care research. The CRC2 will be responsible for managing data related to study outcomes, ensuring that all source documents are complete and that participants adhere to study protocols, especially those specific to the ICU and OR environment. Regular collaboration with medical teams, including nurses and pharmacy staff, will be essential.

At Stanford University School of Medicine, the work we do touches the lives of those today and tomorrow. Through education, research, and health care, the School of Medicine improves health through leadership, diversity, collaborative discoveries, and innovation in health care. Whether working in departments with faculty, or in units that support the school, our staff are a part of teams that propel us on our journey toward the future of medicine and Precision Health.

Stanford is rooted in a culture of excellence and values innovation, collaboration, and life‑long learning. To foster the talents and aspirations of our staff, Stanford offers career development programs, competitive pay that reflects market trends, and benefits that increase financial stability and promote healthy, fulfilling lives. An award‑winning employer, Stanford offers an exceptional setting for professionals looking to advance their careers.

The School of Medicine and the Department of Anesthesia are committed to diversity, equity, and inclusion for its faculty, staff, residents, postdocs, and fellows. We aim to recruit, support, retain, and promote diversity in our department.

For more information on our department, please see our website: https://med.stanford.edu/anesthesia.html

Duties include:

• Lead subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining p articipants in long‑term clinical trials.
• Oversee and contribute to data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data.
• Collaborate on project schedules, targets, measurements, and accountabilities, as assigned.
• Train, and /or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work.
• Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions.
• Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.
• Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices.
• Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract.
• Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.
• Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed.
• May require working extended or unusual hours based on research requirements and business needs. This may include weekends and early or late hours.

* - Other duties may also be assigned

The Department of Anesthesiology, Perioperative, and Pain Medicine, at Stanford University’s School of Medicine, is a world‑leading department that offers comprehensive training and perioperative patient care, pain management, and critical care medicine as well as cutting‑edge research, encompassing a wide spectrum of programs in basic, translational, clinical, health services and medical education.

The Department of Anesthesiology, Perioperative, and Pain Medicine is in search of a Clinical Research Coordinator 2 (CRC2) – Fixed‑term 2 years to coordinate a dynamic portfolio of multiple complex clinical trials in various stages of the study life‑cycle, from start‑up through closeout. Participant populations are primarily adult patients in critical care and operative spaces, and will require long‑term outpatient follow‑up. Evolving study portfolio is primarily industry‑sponsored and includes research on treatments for Sepsis, Acute Respiratory Distress Syndrome, and Acute Kidney Injury. The CRC2 will participate in the identification, recruitment, and enrollment of participants. Trial design will sometimes require unusual work hours, including nights and weekends. The CRC2 will collaborate with other team members to collect key study measures, maintaining the integrity of critical care research. The CRC2 will be responsible for managing data related to study outcomes, ensuring that all source documents are complete and that participants adhere to study protocols, especially those specific to the ICU and OR environment. Regular collaboration with medical teams, including nurses and pharmacy staff, will be essential.

At Stanford University School of Medicine, the work we do touches the lives of those today and tomorrow. Through education, research, and health care, the School of Medicine improves health through leadership, diversity, collaborative discoveries, and innovation in health care. Whether working in departments with faculty, or in units that support the school, our staff are a part of teams that propel us on our journey toward the future of medicine and Precision Health.

Stanford is rooted in a culture of excellence and values innovation, collaboration, and life‑long learning. To foster the talents and aspirations of our staff, Stanford offers career development programs, competitive pay that reflects market trends, and benefits that increase financial stability and promote healthy, fulfilling lives. An award‑winning employer, Stanford offers an exceptional setting for professionals looking to advance their careers.

The School of Medicine and the Department of Anesthesia are committed to diversity, equity, and inclusion for its faculty, staff, residents, postdocs, and fellows. We aim to recruit, support, retain, and promote diversity in our department.

For more information on our department, please see our website: https://med.stanford.edu/anesthesia.html

Duties include:

• Lead subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining p articipants in long‑term clinical trials.
• Oversee and contribute to data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data.
• Collaborate on project schedules, targets, measurements, and accountabilities, as assigned.
• Train, and /or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work.
• Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions.
• Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.
• Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices.
• Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract.
• Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.
• Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed.
• May require working extended or unusual hours based on research requirements and business needs. This may include weekends and early or late hours.

* - Other duties may also be assigned

Qualifications:

DESIRED QUALIFICATIONS:

• Experience coordinating complex industry‑sponsored clinical trials in the critical care and OR settings.
• Experience processing and shipping human biological samples in a laboratory environment.
• Experience interacting with healthcare professionals in a critical care environment.

EDUCATION & EXPERIENCE (REQUIRED):

Bachelor's degree in a related field and a minimum of two years of experience in clinical research, or an equivalent combination of education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Experience navigating EMR systems
• Experience coordinating inpatient clinical trials
• Experience recruiting participants and obtaining informed consent in a hospital setting
• Strong interpersonal skills
• Proficiency with Microsoft Office and database applications.
• Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
• Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

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 their 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, aerosols, 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.

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 .

The expected pay range for this position is $84,856 to $97,021 per annum.

Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanford’s extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

• Fixed Term Y
• Stanford Schools and Units School of Medicine
• Full time or Part time Full Time
• Regular or Temporary Regular
• Job Category Research
• Posting Date 04/28/2026, 07:48 PM
• Grade H
• Job Identification 108985

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Benefits that support you, and your future

18+ PTO days per year

Health benefits start when you start

Flexible work options

$6000+ annual tuition and training assistance

403(b) plan

Mental health and wellness programs

Free and discounted commuter transportation

Applies to regular full-time positions.

Notice to Applicants

The job duties listed are typical examples of work performed by positions in this job classifications and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

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 their job.

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

Stanford University provides job pay ranges representing its good faith estimate of what the university reasonably expects to pay for a particular job. The specific pay offered to a selected candidate will be determined based on a wide range of factors that are unique to each candidate, including but not limited to geographic work location, relevant knowledge, skills and abilities, relevant education, years of relevant experience, depth and breadth of relevant experience, and performance; further including but not limited to other business and organization needs such as the scope and responsibilities of the position, the minimum qualifications, departmental budget availability, and market and internal equity across the university, school/ unit, department, as well as job reporting relationshipships.

Why work at Stanford

World-changing work in a culture of continuous learning

An inspiring community that values collaboration

High-quality health and wellness benefits that put you and your family first

Access to world-class education and career development, with tuition reimbursement, training assistance, and more