Clinical Research Study Coordinator

Bronx, New York

Posted in Health and Safety
5 days ago

Job Info

34 MARCONI STSuite 120, Bronx, New York, 10461-2710, United States of America

DaVita Clinical Research (DCR), a wholly owned subsidiary of DaVita Inc., is the research arm of DaVita. DCR innovates through retrospective outcomes research aimed at improving care and quality of life for people with kidney disease. DCR assists pharmaceutical and medical device companies in the design, recruitment and completion of clinical trials using its renal research site network. For 30 years we have helped 500+ clients with their development projects. DCR is based in Minneapolis, MN and operates in locations across the US.

The Clinical Research Study Coordinator coordinates and conducts clinical research trials in DCR's Alliance Site Network sites. They may manage Research Assistants at the site if there is not a Sr Administrator or Regional Research Manager.

This position will be based out of our Bronx office and will coordinate and execute all aspects of late phase clinical trials in the Bronx, NY area.

  • ​​


    • Accountable for the successful execution of clinical trials through all phase of the study: enrollment, maintenance and close out.

    • Responsible for performing research procedures according to the study protocol and working in partnership with the physician investigator to coordinate research activities.

    • Serves as a liaison between the physicians (Principal Investigator or Sub-Investigator), study sponsors and DaVita facility teammates.

    • Responsible to deliver or exceed project enrollment targets for clinical research studies at their site.

    • Responsible for accurate and timely data entry into the electronic data entry systems.

    • Responsible for timely resolution of all data queries to meet project timelines for database lock.

    • Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law.

    • Demonstrates adherence to DCR standard operating procedures and policies and with the standards customary in the clinical research industry.

    • Understands and promotes compliance with all applicable healthcare and research regulations.


    • Bachelor's degree or equivalent experience required.

    • Minimum 2 years of experience as a clinical research coordinator is strongly preferred. Must have experience with late phase drug and device trials (phase 2, 3, 4).

    • Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.

    • Commitment to and role model of DaVita's values with ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactions

    • Travel required up to 10% depending on business needs.

    • Experience in managing confidential information and/or issues using discretion and judgment.

    Here is what you can expect when you join our Village:
    * A "community first, company second" culture based on Core Values that really matter.
    * Clinical outcomes consistently ranked above the national average.
    * Award-winning education and training across multiple career paths to help you reach your potential.
    * Performance-based rewards based on stellar individual and team contributions.
    * A comprehensive benefits package designed to enhance your health, your financial well-being and your future.
    * Dedication, above all, to caring for patients suffering from chronic kidney failure across the nation.

    Join us as we pursue our vision "To Build the Greatest Healthcare Community the World has Ever Seen."
    Why wait? Explore a career with DaVita today.
    Go to to learn more or apply.

    Join us as we pursue our vision "To Build the Greatest Healthcare Community the World has Ever Seen."

    Why wait? Explore a career with DaVita today.

    Go to to learn more or apply.

At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed Diversity & Belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and an affirmative action employer. As such, individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.

Salary/ Wage Range

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies and experience and may fall outside of the range shown. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at

More Health and Safety jobs

Cantex Health Care Centers LLC
Round Rock, Texas
Posted 40 minutes ago

Cantex Health Care Centers LLC
Dallas, Texas
Posted 40 minutes ago

Cantex Health Care Centers LLC
Livingston, Texas
Posted 40 minutes ago
View Health and Safety jobs »

Job Alerts

Provide an email, zip code for jobs, and/or job category to subscribe to job alerts. Learn more now.

Share this job with the community

Click a community link below, and then social share the Clinical Research Study Coordinator job.

African American Job Search Logo
Asian Job Search Logo
Disabled Job Seekers Logo
Hispanic Job Exchange Logo
LGBT Job Search Logo
Seniors to Work Logo
US Diversity Job Search Logo
Veteran Job Center Logo