U.S. Dermatology Partners · 6 hours ago
Clinical Research Coordinator I
Phoenix, AZ
Full-time
Onsite
New Grad, Entry Level
$55K/yr - $65K/yrU.S. Dermatology Partners is a healthcare organization focused on dermatological services, and they are seeking a Clinical Research Coordinator I. The role involves executing study-related activities under the supervision of a physician, ensuring compliance with clinical protocols and managing patient interactions throughout the clinical trial process.
Health CareHospitalMedicalWellness
Responsibilities
Maintain all aspects of study protocol during recruitment, screening, enrollment, and follow-up visits
Assist the PI, and team when applicable, the informed consent process with patients and their families
Conduct and coordinate patient visits including patient demography, vitals, EKG, phlebotomy, photography, administering investigational drug, assisting PI and sub-investigators with physical exam, and scheduling appropriate follow-up visits
Communicate frequently with contract research organizations, IRB, Sponsors, Central Lab Facilities, and other outside vendors to manage the day-to-day needs for current and prospective trials
Maintain all source documents and investigational drug accountability records
Enter source data into EDC efficient and accurately
Maintain regulatory documents related to ISF
Follow SOPs, policies, and procedures as set forth by the company
Review EDC for accuracy and completion, and resolve queries as they arise
Assists with direct patient care procedures, as required by the study, including biopsies, surgeries, cosmetic procedures and related tasks
Process prescriptions and prior authorizations as directed by physician. Address patient and/or pharmacy questions concerning medication. Enroll patients in patient education/assistance programs
Ensure necessary study related documentation and correspondence study subjects, study teams, vendors, and sponsors
Scans correspondence into EMR
Practices safety, environmental, and/or infection control methods
Assist clinical research manager in delegated tasks
Performs miscellaneous job-related duties as assigned
Process blood and urine samples in accordance with IATA and OSHA standards
Prepare necessary documentation for SIV, IMV, COVs and other sponsor related meetings
Working knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol
Qualification
Required
Under the general supervision of a physician and the clinical and clinical research team in an outpatient setting
Responsible for executing study-related activities from study startup through closeout
Conducted in compliance with Good Clinical Practice (GCP), ALCOA-C principles, sponsor requirements, and USDP standards
Support the Principal Investigator in the conduct of clinical trial visits
Ensure that participants are appropriately scheduled and that all protocol-specified procedures are completed accurately and in a timely manner
Maintain all aspects of study protocol during recruitment, screening, enrollment, and follow-up visits
Assist the PI, and team when applicable, the informed consent process with patients and their families
Conduct and coordinate patient visits including patient demography, vitals, EKG, phlebotomy, photography, administering investigational drug, assisting PI and sub-investigators with physical exam, and scheduling appropriate follow-up visits
Communicate frequently with contract research organizations, IRB, Sponsors, Central Lab Facilities, and other outside vendors to manage the day-to-day needs for current and prospective trials
Maintain all source documents and investigational drug accountability records
Enter source data into EDC efficient and accurately
Maintain regulatory documents related to ISF
Follow SOPs, policies, and procedures as set forth by the company
Review EDC for accuracy and completion, and resolve queries as they arise
Assist with direct patient care procedures, as required by the study, including biopsies, surgeries, cosmetic procedures and related tasks
Process prescriptions and prior authorizations as directed by physician
Address patient and/or pharmacy questions concerning medication
Enroll patients in patient education/assistance programs
Ensure necessary study related documentation and correspondence study subjects, study teams, vendors, and sponsors
Scans correspondence into EMR
Practices safety, environmental, and/or infection control methods
Assist clinical research manager in delegated tasks
Perform miscellaneous job-related duties as assigned
Process blood and urine samples in accordance with IATA and OSHA standards
Prepare necessary documentation for SIV, IMV, COVs and other sponsor related meetings
Working knowledge, at minimum, of all applicable protocols
Company
U.S. Dermatology Partners
U.S.Dermatological Partners' integrated care network gives dermatology clinics access to general medical, surgical, and skin treatments.
Founded in 2012
1001-5000 employees
Funding
Current Stage
Late StageTotal Funding
unknown2016-05-19Acquired
Leadership Team
Gurpal (Paul) Singh
Chief Executive Officer
Brian Bernholtz
Chief Financial Officer
Recent News
2025-12-19
2025-12-18
2025-12-02
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