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Clinical Research Coordinator II - Cardiology

Washington University in St. Louis
Posted a month ago, valid for 17 days
Location

Ann Arbor, MI 48113, US

Salary

$52,600 - $78,900 per year

Contract type

Full Time

Health Insurance
Employee Assistance

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Sonic Summary

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  • The Cardiovascular Division at Washington University School of Medicine is seeking a Clinical Research Coordinator II (CRC II) to oversee global cardiovascular health research initiatives.
  • The position requires a Bachelor's degree and at least 2 years of clinical research experience, with a salary range of $52,600 to $78,900 annually.
  • The CRC II will manage day-to-day operations of multiple studies, ensuring compliance with regulatory requirements and maintaining data integrity.
  • Key responsibilities include coordinating study protocols, preparing regulatory documentation, and assisting with financial and administrative support for research projects.
  • Candidates must obtain Basic Life Support certification within one month of hire and possess strong organizational and communication skills.

Scheduled Hours

40

Position Summary

The Cardiovascular Division in the Department of Internal Medicine at Washington University School of Medicine is seeking a highly organized and experienced Clinical Research Coordinator II (CRC II) to support funded global cardiovascular health research and research training initiatives. Working under the direction of the Principal Investigator (PI), the CRC II will independently coordinate and manage complex clinical research activities across multiple studies, ensuring regulatory compliance, data integrity, and efficient study execution.
This role serves as a key operational lead and liaison among the PI, study teams, institutional offices, sponsors, and external collaborators. The ideal candidate will be proactive, detail-oriented, and capable of managing competing priorities while supporting regulatory, administrative, financial, and operational aspects of clinical research projects.

Job Description

Primary Duties & Responsibilities:

Study Operations & Coordination

  • Independently coordinate and manage day-to-day operations of multiple funded clinical research studies, including domestic and international projects.
  • Implement and oversee all phases of assigned study protocols in accordance with institutional policies, study timelines, and regulatory requirements.
  • Serve as a primary liaison between the PI, study teams, sponsors, collaborators, and institutional stakeholders.
  • Coordinate study start-up activities, including protocol development, study materials, case report forms, and standard operating procedures (SOPs).
  • Assist with training and oversight of research staff, students, and trainees involved in study activities.

Regulatory & Compliance

  • Prepare, submit, and maintain regulatory documentation, including IRB applications, continuing reviews, amendments, reportable events, and protocol deviations.
  • Ensure compliance with institutional, federal, and sponsor requirements, including ICH-GCP and NIH policies.
  • Maintain accurate and organized regulatory binders and study records.
  • Navigate and manage federal and institutional research platforms, including ClinicalTrials.gov PRS, eCONNECT, and other NIH systems, as applicable.
  • Monitor study conduct and identify compliance issues; recommend and implement corrective actions in consultation with the PI.

Data Management & Reporting

  • Oversee data collection, quality control, and documentation to ensure accuracy and completeness.
  • Evaluate and interpret collected clinical and research data as appropriate.
  • Prepare written and oral progress reports, summaries, and analyses for the PI, sponsors, and regulatory bodies.
  • Assist with preparation of manuscripts, abstracts, and presentations for peer-reviewed publications and scientific meetings.

Financial & Administrative Support

  • Assist with study budget development, tracking, and forecasting.
  • Coordinate invoicing, subcontractor documentation, and expense reconciliation in collaboration with departmental and institutional partners.
  • Support PI with administrative components of funded projects, including NIH RPPR-related documentation, as needed.

Additional Responsibilities

  • Conduct literature reviews to support study planning and protocol development.
  • Assist with grant proposal preparation and modifications to study design, as appropriate.
  • Perform other duties as assigned in support of research and programmatic goals.

Working Conditions:

Job Location/Working Conditions

  • Office space / dry lab

Physical Effort

  • Typically sitting at desk or workstation

Equipment

  • Standard office equipment

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications

Education:

Bachelor’s degree or combination of education and/or experience may substitute for minimum education.


Certifications/Professional Licenses:

The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.

Basic Life Support - American Heart Association, Basic Life Support - American Red Cross


Work Experience:

Clinical Research (2 Years)


Skills:

Not Applicable


Driver's License:

A driver's license is not required for this position.

More About This Job

Required Qualifications

  • Basic Life Support certification must be obtained within one month of hire date.
  • Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).

Preferred Qualifications

Education:

No additional education unless stated elsewhere in the job posting.


Certifications/Professional Licenses:

No additional certification/professional licenses unless stated elsewhere in the job posting.


Work Experience:

No additional work experience unless stated elsewhere in the job posting.

Skills:

Clinical Research, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)

Grade

C10

Salary Range

$52,600.00 - $78,900.00 / Annually

The salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.

Questions

For frequently asked questions about the application process, please refer to our External Applicant FAQ.

Accommodation

If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.

All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.

Pre-Employment Screening

All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.

Benefits Statement

Personal

  • Up to 22 days of vacation, 10 recognized holidays, and sick time.

  • Competitive health insurance packages with priority appointments and lower copays/coinsurance.

  • Take advantage of our free Metro transit U-Pass for eligible employees.

  • WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.

Wellness

  • Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!

Family

  • We offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We’ve got you covered.

  • WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.

For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/

EEO Statement

Washington University in St. Louis is committed to the principles and practices of equal employment opportunity and especially encourages applications by those from underrepresented groups. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information.

Washington University is dedicated to building a community of individuals who are committed to contributing to an inclusive environment – fostering respect for all and welcoming individuals from diverse backgrounds, experiences and perspectives. Individuals with a commitment to these values are encouraged to apply.



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