Enable job alerts via email!

Clinical Research Coordinator

Davita Inc.

Saint Paul (MN)

On-site

USD 48,000 - 63,000

Full time

8 days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

A leading healthcare organization is seeking a Clinical Research Coordinator who will manage day-to-day research activities within the Departments of Surgery and Radiology. The role involves recruiting participants, coordinating study operations, and ensuring compliance with research protocols. Candidates should have a BA/BS degree and strong communication skills. Competitive salary and benefits package offered.

Benefits

Health insurance
Retirement plans
Paid time off
Tuition support

Qualifications

  • A Bachelor's degree or equivalent experience is required.
  • Excellent communication skills and the ability to work independently and flexibly.
  • Preferred: Experience with clinical research and familiarity with medical terminology.

Responsibilities

  • Manage day-to-day study activities including participant screening and consent.
  • Coordinate study activities and ensure protocol compliance.
  • Facilitate communication among research team members and train staff.

Skills

Communication
Flexibility
Proficiency in software applications

Education

BA/BS degree or equivalent experience

Job description

The job description is quite detailed but contains excessive formatting tags and some redundant information. To improve readability and professionalism, the description should be reformatted using only necessary HTML tags such as

,

,
    ,
  • , , and
    . The content should be condensed to focus on key responsibilities, qualifications, and application instructions, removing repetitive or overly detailed sections that do not add value for potential applicants. Here's a refined version:
    About the Job

    The Clinical Research Coordinator works under the supervision of the Program Manager(s) and is responsible for managing day-to-day study activities, including participant screening, consent, study visits, data entry, and biospecimen management. This role supports multiple study protocols within the Departments of Surgery and Radiology, involving observational and interventional research projects.

    Job Duties
    • Screen and recruit participants, obtain consent, and educate families about the research process.
    • Coordinate study activities, ensure protocol compliance, and manage biospecimen collection and shipment.
    • Abstract and enter data, maintain documentation, and respond to data queries.
    • Facilitate communication among research team members and train staff on study protocols.
    • Perform other duties as assigned, including database management and supporting special projects.
    Qualifications

    Required qualifications include a BA/BS degree or equivalent experience, proficiency in software applications, excellent communication skills, and the ability to work independently and flexibly. Preferred qualifications include experience with clinical research, familiarity with medical terminology, and certifications such as CCRC or CCRP.

    About the Department

    The Department of Surgery is committed to innovation, diversity, and excellence in education, research, and patient care. Learn more at https://med.umn.edu/surgery.

    Pay and Benefits

    Salary ranges are $48,000 - $56,000 for RP1RC and $56,000 - $63,000 for RP2RC, depending on experience. Benefits include health insurance, retirement plans, paid time off, tuition support, and more. Details are available on the University HR website.

    How to Apply

    Apply online by submitting your application, cover letter, and resume. Additional documents can be uploaded via your application portal. For accommodations, contact employ@umn.edu or call (612) 624-8647.

    Diversity and Equal Opportunity

    The University values diversity and is an equal opportunity employer. We encourage applicants from all backgrounds to apply. More information at http://diversity.umn.edu.

    Employment Requirements

    Employment is contingent upon a background check. Criminal history does not automatically disqualify applicants.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Clinical Research Coordinator B

University of Pennsylvania

null null

Remote

Remote

USD 52,000 - 53,000

Full time

8 days ago

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Medpace

Phoenix null

Remote

Remote

USD 60,000 - 80,000

Full time

10 days ago

Clinical Research Coordinator I (Hybrid) - Radiology

Washington University in St. Louis

null null

Remote

Remote

USD 60,000 - 80,000

Full time

8 days ago

Clinical Research Coordinator

Highlands Oncology Group PA in

Springdale null

On-site

On-site

USD 60,000 - 75,000

Full time

Yesterday
Be an early applicant

Clinical Research Coordinator

Neurology Consultants of Dallas

Dallas null

On-site

On-site

USD 50,000 - 75,000

Full time

Today
Be an early applicant

Clinical research coordinator

Washington University in St Louis

St. Louis null

On-site

On-site

USD 47,000 - 72,000

Full time

Today
Be an early applicant

Clinical Research Coordinator I - Radiology

Washington University in St. Louis

St. Louis null

On-site

On-site

USD 62,000 - 97,000

Full time

5 days ago
Be an early applicant

Clinical Research Coordinator

Cedar Health Research

Euless null

On-site

On-site

USD 55,000 - 80,000

Full time

4 days ago
Be an early applicant

Clinical Research Coordinator II- Dallas Presby

Davita Inc.

Dallas null

On-site

On-site

USD 55,000 - 85,000

Full time

7 days ago
Be an early applicant