"Alerted.org

Clinical Research Coord I

Work type: Staff Full-Time

Categories: Office/Administrative/Fiscal Support, Health Care Administration/Support

Department: 29050903 - MD-PULMONARY-OTHER

Classification Title:

Clinical Research Coordinator I

Classification Minimum Requirements:

Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.

Job Description:

The Department of Medicine, Division of Pulmonary is seeking a full time Clinical Research Coordinator I. This position will function in clinical research setting and will, under moderate supervision, coordinate assigned clinical research activities. The incumbent must demonstrate effective problem-solving, writing, and communication skills. The incumbent will be directly involved with research activities related to industry-sponsored clinical trials/research within the Division of Pulmonary, Critical Care & Sleep Medicine and ensure compliance with federal, state, and university policies. The CRC I supports study investigators by handling day-to-day study tasks (e.g. scheduling and data entry) and ensures compliance with study protocols and regulatory guidelines, while safeguarding participant safety.

Essential Functions;

Clinical Trial Project Management

Schedule and organize participant appointments, study visits, and protocol-related procedures, maintaining adherence to IRB-approved protocols and follow-up care plans. Assist with patient recruitment and screening and participate in the informed consent process under the guidance of investigators and senior staff. Maintain accurate study documentation and source data. Complete case report forms and enter data into electronic data capture (EDC) systems, promptly addressing any data queries. Collect, process, and ship laboratory specimens (e.g. blood samples) per protocol requirements. Ensure all samples and study materials are handled and shipped according to study and safety guidelines.

Clinical trial support

Perform general study support tasks, including reporting adverse events, upholding Good Clinical Practice (GCP) standards, and complying with institutional policies and study-specific standard operating procedures. This may include assisting in maintaining regulatory binders and essential documents under supervision.

This position will perform ad hoc assignments as assigned by the Supervisor.

Expected Salary:

$43,888 - $52,600 Annually

Required Qualifications:

Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.

Preferred:

Bachelor’s degree in a life science, a health science, or related field. Prior experience in a clinical research setting (especially in pulmonary or respiratory studies) beyond the required years is strongly preferred. Familiarity with electronic data capture systems and IRB procedures is a plus. Professional clinical research certification (e.g., ACRP or SOCRA credentials) is advantageous, as it demonstrates commitment to research compliance and best practices.

Special Instructions to Applicants:

In order to be considered, you must upload your resume.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Health Assessment Required:No

Advertised: 29 May 2025 Eastern Daylight Time

Applications close: 06 Jun 2025 Eastern Daylight Time