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Kidney Research Jobs (NOW HIRING)

Uw

Research Coordinator 1

Seattle, WA · On-site

$90K/yr

The Kidney Research Institute in the Department of Medicine, Division of Nephrology has an excellent opportunity for a Research Coordinator 1 to join their team. About this Opportunity The research ...

University of Pennsylvania

Temp - Research Asst

Center, TX · On-site

$7.25 - $25/hr

This temporary position will provide part-time laboratory and data support for ongoing kidney research studies, including tissue processing, data organization, and assistance with molecular biology ...

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As of Jul 12, 2026, the average hourly pay for kidney research in the United States is $40.32, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $50.48 per hour, depending on experience, location, and employer.

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A Kidney Research job involves studying kidney function, diseases, and treatments to improve patient outcomes. Researchers may work in laboratories, hospitals, or academic institutions, conducting experiments, analyzing data, and developing new therapies. The role often requires collaboration with healthcare professionals, writing scientific papers, and securing research funding.

What are the key skills and qualifications needed to thrive in the Kidney Research position, and why are they important?

To thrive in Kidney Research, a strong background in biomedical sciences or a related field, often at the Master's or PhD level, and experience with clinical or laboratory research methodologies is essential. Familiarity with laboratory instruments, data analysis software such as SPSS or R, and research compliance certifications like CITI training are typically required. Excellent analytical thinking, problem-solving skills, and the ability to collaborate within multidisciplinary teams help professionals excel in this field. These competencies are crucial to ensure high-quality, ethical research outcomes that advance kidney health and patient care.

What does a typical workday look like for someone in Kidney Research?

A typical workday in Kidney Research may involve designing and conducting experiments, analyzing biological samples, and reviewing data to uncover new insights about kidney function and disease. Researchers also spend time writing reports or scientific articles, attending team meetings, and collaborating closely with clinicians, bioinformaticians, and laboratory staff. The environment may shift between laboratory, hospital, and office settings, depending on the specific project phase. You'll also be expected to stay current with medical literature and regulatory requirements to ensure research integrity. This combination of hands-on research, data analysis, and teamwork makes each day varied and intellectually stimulating for those passionate about advancing kidney health.

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Project Manager/Research Coordinator 3 (Temporary)

Project Manager/Research Coordinator 3 (Temporary)

University of Washington

Seattle, WA • On-site, Remote

Full-time

Re-posted 25 days ago

University Of Washington School Of Medicine rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

179th of 552 rated colleges and universities

Job description

Job Description
The Kidney Research Institute (KRI) has an excellent opportunity for a temporary Project Manager/Research Coordinator 3 to provide expert level lead support for multi-funded and multi-site clinical research studies involving human subjects with kidney disease and related conditions.
This position requires working directly with KRI investigators, KRI staff, and collaborators outside of the University of Washington on a wide range of scientific research projects related to kidney disease. The Kidney Research Institute functions as the research arm within the Nephrology Division of the UW Department of Medicine with a goal of conducting innovative clinical research to improve the health and quality of life of persons with renal disease and related conditions. The Project Manager will have a vital role in the progression of research at the KRI.
DUTIES AND RESPONSIBILITIES
Project Management:
  • Independently coordinate and oversee multiple data collection efforts for multiple complex research projects which may include other collaborating agencies or institutions.
  • Oversee and coordinate the transmission of samples and data between collaborators/institutions.
  • Develop and prepare annual reports, center reports, grant submission components, JIT materials for principal investigators, industry sponsors and institutional review board to ensure that each project is moving toward timely completion.
  • Serve as the primary liaison between the project team and funding agencies or significant parties and for complex regulatory or compliance matters.
  • Ensure timely execution of research activities in alignment with project milestones, timelines, and research objectives.
  • Implement investigative research protocols and monitor adherence to protocol; troubleshoot and resolve problems such as deviation from protocol requirement.
  • Establish, manage, and improve study workflows and quality standards.
  • Provide leadership, training, and supervision for research staff as needed.
  • Coordinate with KRI managers and other study site personnel for multi-site studies, and coordinate calls/meetings related to studies.
  • Lead short- and long-term study planning collaborating with PI and study team to track timelines and progress towards milestones, deliverables and other study tasks).
  • Support study team with various research activities as needed.

Manage Regulatory and Start-Up Activities:
  • Provide expert level regulatory and compliance support, and ensure compliance with IRB requirements.
  • Lead preparation of human subject applications, consent forms, and modifications in compliance with Institutional Review Board (IRB) requirements.
  • Ensure adherence to research protocols and verify accuracy of research study data.
  • Responsible for adverse events collection and reporting to IRB, FDA, other fed agencies, sponsors, clinical trials.gov.
  • Oversee and ensure compliance with IRB and VA R&D regulations and trainings for all research staff.
  • Lead audit preparation and facilitation (internal or sponsor initiated).
  • Design/write case report forms - promote consistent data capture and successful statistical analysis; develop research protocols and procedures; develop data dictionaries, merge data sets.
  • Contribute to the development of procedures for the design of measurement instruments and scoring systems.
  • Authoring technically detailed scientific documentation and study materials appropriate for a general audience and clinical/technical audience.
  • Manage all areas of the study start-up process.
  • Collaborate with sponsor/external party to satisfy all site activation requirements.
  • Obtain approvals for study-related procedures such as laboratory, imaging, research space, etc.
  • Conduct and create process improvement of study protocols and materials.
  • Review and resolve complex billing issues; oversee CPT coding accuracy.
  • Collaborate with UW Clinical Trials Office (CTO) to develop, negotiate, and finalize budgets and billing procedures.
  • Managing studies in OnCore Clinical Trials Management System (CTMS).

Communication and Reporting:
  • Independently prepare and present study updates to investigators, funders, advisory committees, and stakeholders.
  • Collaborate with the PI to prepare sponsor reports, e.g. RPPR, DSMB.
  • Oversee the preparation of recruitment reports locally and across sites, with Research Coordinators and others.
  • Maintain highly organized shared folders, calendars and other information management tools with a high degree of attention to detail.
  • Provide administrative leadership support for internal study team (e.g., host meetings, draft meeting minutes, and communicate action items).
  • Serve as primary point of contact for study team and other UW stakeholders.
  • Develop and maintain external communication and study support materials.
  • Contribute to KRI-wide communications efforts and external engagement.

MINIMUM REQUIREMENTS
Bachelor's degree in a related field and four years of relevant experience.
Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration.
Additional Requirements:
  • Strong interpersonal skills and flexibility to work with personnel at various levels in a cross-institutional research environment.
  • Demonstrated ability to lead the implementation of complex research protocols and maintain high standards of accuracy, timeliness and professionalism.
  • Demonstrated ability in ensuring security and confidentiality of study materials.
  • High level of competency, good judgment, discretion in carrying out tasks, troubleshooting problems and following through on projects to meet deadlines and study benchmarks.
  • Proven experience demonstrating a high degree of organizational skills with a high degree of attention to details Proven reliability and flexibility to work independently and function as a lead in directing the work of a diverse team.
  • Prior experience in a laboratory or clinical research environment to facilitate interactions between laboratory staff, research coordinators and research staff.
  • Thorough knowledge of HIPAA, IRB and related institutional requirements for the conduct of research.
  • Experience working with the UW, VA and HMC setting.
  • Strong verbal and written communication skills.
  • Ability to commute between various sites: UWMC, NKC, HMC, etc
  • Basic biostatistical and epidemiological principles/methods, STATA or similar statistical software Certified.
  • Research Coordinator (CCRC), Association of Clinical Research Professionals.
  • Research Electronic Data Capture (Redcap) and Bio-repository database experience.
  • Familiarity and experience with kidney disease and related illnesses.

DESIRED REQUIREMENTS
  • MPH, MS Epi, or related graduate degree.

#UWDeptMedicineJobs
Compensation, Benefits and Position Details
Pay Range Minimum:
$78,600.00 annual
Pay Range Maximum:
$130,668.00 annual
Other Compensation:
Benefits:
For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-temporary-per-diem-and-less-than-half-time/
Shift:
First Shift (United States of America)
Temporary or Regular?
This is a temporary position
FTE (Full-Time Equivalent):
100.00%
Union/Bargaining Unit:
Not Applicable
About the UW
Working at the University of Washington provides a unique opportunity to change lives - on our campuses, in our state and around the world.
UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.
Our Commitment
The University of Washington is committed to fostering an inclusive, respectful and welcoming community for all. As an equal opportunity employer, the University considers applicants for employment without regard to race, color, creed, religion, national origin, citizenship, sex, pregnancy, age, marital status, sexual orientation, gender identity or expression, genetic information, disability, or veteran status consistent with UW Executive Order No. 81.
To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or dso@uw.edu.
Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law.

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