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Clinical Research Coordinator I - Rollins School of Public Health

Role overview

Qualifications

  • High School Diploma or GED and three years of administrative support experience
  • Two years of college in a scientific, health-related, or business administration program and one year of admin support or customer service experience
  • Licensed practical nurse (LPN) with one year of admin support or one year of licensed practical nursing experience
  • Bachelor's degree, Master's degree, MD or PhD in a scientific, health-related or business administration program

Responsibilities

  • Maintain data pertaining to research projects, complete source documents/case report forms, and perform data entry
  • Assist with patient recruitment and attend study meetings
  • Collect study specimens according to protocol, which may include phlebotomy and processing
  • Schedule, coordinate, and oversee study visits with research participants, including conducting informed consent processes and administering questionnaires

Key facts

Hard skills

Other skills

  • Quality Assurance
  • Communication
  • Teamwork
  • Reliability
  • Proactivity

About the company

Emory Healthcare logo

Emory Healthcare

Hospitals & Health Care

Emory Healthcare is the most comprehensive health care system in Georgia. We offer 11 hospitals, the Emory Clinic, more than 250 provider locations, and more than 2,800 physicians specializing in 70 different medical subspecialties. Meaning we can provide treatments and services that may not be available at local community hospitals. That's the Emory Difference.

Company details

Company typeXLarge
IndustryHospitals & Health Care
Company size10001

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Job description

Discover Your Career at Emory University: Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. Description:

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.

KEY RESPONSIBILITIES:

  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.

ADDITIONAL JOB DETAILS:

The full-time (40 hours/week) Clinical Research Coordinator (CRC) will support a 5-year clinicalresearch study funded by the National Institute of Environmental Health Sciences (NIEHS)Superfund Research Program (SRP). The study examines relationships between chemical exposuresand health outcomes in adults residing in Glynn County, Georgia.


The CRC will be the primary on-the-ground presence for study operations in Glynn County and willserve as an essential point of contact for study participants. The CRC should be highly organized,proactive, reliable, and willing to work on the occasional night or weekend. This is a locally basedposition; candidates must reside in or be willing to relocate to the Glynn County, GA area. The CRCwill report to the study investigators at Emory University’s Rollins School of Public Health and willwork closely with other team members.


The successful candidate will be responsible for scheduling, coordinating, and overseeing studyvisits with research participants. This includes conducting informed consent processes,administering questionnaires, collecting and managing biological specimens, and maintaining allrequired study documentation. The CRC will be expected to follow protocols and applicable safety,ethical, and regulatory requirements, maintain accurate and organized study records, and performroutine data quality checks.


Candidates should be comfortable working independently in a field-based research environmentwhile collaborating closely with a larger research team. Although the position is based in GlynnCounty, the CRC will interact regularly with the Research Project Manager and study investigators atEmory to provide updates on field operations, identify and resolve issues, and ensure consistentimplementation of study protocols. The position also requires the ability to collect, store, and shipbiological specimens and to communicate effectively with study participants and research staff.Occasional travel to Atlanta for team meetings or professional development activities is possibleand will be covered by the study.


An essential job requirement is that the CRC can build and maintain trusted relationships with studyparticipants and community partners in Glynn County to support participant retention and to fulfillthe value of community-engaged research.

MINIMUM QUALIFICATIONS:

  • High School Diploma or GED and three years of administrative support experience.
  • Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
  • Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
  • Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.

This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.

PREFERRED QUALIFICATIONS:

  • Knowledge and understanding of health research and clinical research projects.
  • Experience working in community-based or clinical human subjects research, or other relevantproject management experience.
  • Experience with biological specimen collection, processing, and/or shipping (includingphlebotomy certification or willingness to obtain).
  • Demonstrated ability to maintain accurate study records and ensure data quality, includingcompletion of required documentation and routine quality-control checks.

NOTE: This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University location as needed.  All biweekly employees must reside within the State of Georgia.  Emory reserves the right to change this status with notice to employee.

Additional Details: Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).

Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.

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Marcus Rivera

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