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Clinical Research Coordinator

Job in Richmond, Henrico County, Virginia, 23214, USA
Listing for: Commonwealth of VA Careers
Full Time position
Listed on 2026-07-22
Job specializations:
  • Research/Development
    Clinical Research
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 52500 - 55000 USD Yearly USD 52500.00 55000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Coordinator 621500

Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU’s sponsored research, the School of Medicine is internationally recognized for patient care and education. Virginia Commonwealth University is an equal opportunity employer.

Unit:
School Of Medicine

Department:
Psychiatry

Position Responsibilities

The Clinical Research Coordinator will perform administrative and technical work in support of the research mission of the Child and Adolescent Division in the Department of Psychiatry. The Clinical Research Coordinator is responsible for managing research studies in a compliant and efficient manner. Under the supervision of the Principal Investigator and project manager, the incumbent will collaborate with all members of the research teams, to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and ethical obligations are kept.

  • Under direction of PI, conduct and oversee grants and coordinate research activities by preparing human assurance protocols, informed consent documents, and other research‑related papers
  • Under direction of PI, oversee grant development by performing data collection and entry in compliance with HIPAA, GCP’s and sponsor required guidelines
  • Participate in project planning and development of research protocols while ensuring adherence to accepted scientific research principles and compliance with relevant federal guidelines
  • Conduct all assigned activities in compliance with national, local, & institutional guidelines, according to all HIPAA, GCP, and other applicable requirements
  • Coordinate new study activation requirements, screen/enroll participants, regulatory and compliance requirements, maintain appropriate study documentation/records, and manage study data
  • Conduct clinical research activities as authorized by the Principal Investigator’s documented Delegation of Authority and Training Logs
  • Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), plus additional sponsor GCP certifications as required
  • Understand, adhere to, and assist in developing/submitting IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols
  • Provide analytical writing and training support for projects
  • Coordinate and research scientific literature, evaluate, and summarize findings, and assist PI in developing techniques based on findings
  • Perform all other research duties as assigned
Qualifications

Minimum Qualifications
  • Demonstrated knowledge and understanding of clinical research management, including regulatory, human subjects’ protection, study conduct, and data management requirements
  • Extensive knowledge of ethical research issues and research protocols and guidelines
  • Strong communication skills, both written and verbal, and excellent interpersonal/organizational skills
  • Strong interpersonal skills such as establishing rapport, maintaining participant motivation, empathic responding, ability to work effectively as part of a multidisciplinary team, and ability to use clinical judgment in (rare) emergency situations
  • Working knowledge of Microsoft Office and SPSS or comparable programs
  • Self‑motivated, able to work independently, and familiar with research regulations
  • Ability to read, interpret, and apply complex regulations, policies, and requirements for each study assigned
  • Demonstrated ability to work in and foster an environment of respect, professionalism, and civility with a population of faculty, staff, and students from various backgrounds and experiences, or commitment to do so as a staff member at VCU
Preferred Qualifications
  • Bachelor’s or Master’s of Science degree or equivalent in Psychology, Social Work, or related field
  • Work experience in an academic medical center or university
  • Familiarity with EPIC
  • Phlebotomy Certification
  • Experience conducting research in pediatric or adolescent populations
  • Experience administering surveys in REDCap
  • Experience in conducting mental health surveys with adults and youth
  • Experience with fNIRS
  • Computational skills
Salary Range

$52,

Benefits

All full‑time university staff are eligible for VCU’s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave, generous tuition benefits, retirement planning and savings options, tax‑deferred annuity and cash match programs, employee discounts, well‑being resources, abundant opportunities for career development and advancement, and more.

FLSA Exemption Status

Exempt

Hours per Week

40

Restricted Position

Yes

ORP Eligible

No

Flexible Work Arrangement

Fully Onsite

University Job Title

34111N - Clinical Research Coordinator 1

Contact Information

Name:
Lisa Straub

Email: lkstraub

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