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Clinical Research Coordinator
1 month ago
The Commonwealth of Virginia's VCU Institute for Drug and Alcohol Studies is seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team. As a Clinical Research Assistant, you will play a critical role in supporting the conduct of clinical research trials, ensuring the integrity and quality of research data, and collaborating with the research team to achieve research objectives.
Key Responsibilities:
* Assist in the development and implementation of clinical research protocols, including casefinding, evaluation, and abstraction of source documentation, case report form completion, and database management.
* Collaborate with the research team to ensure compliance with federal, state, and local regulatory requirements, as well as institutional operational research objectives and ethical obligations.
* Develop and maintain productive relationships with VCU colleagues, affiliate sites, and other stakeholders to achieve essential research outcomes.
Requirements:
* Bachelor's degree in Psychology, Neuroscience, or a related field.
* Proficient in computer skills, including word processing, data entry, spreadsheet, database management, and entry-level statistical/programming skills.
* Strong clinical skills, including fundamental clinical skills such as establishing rapport, maintaining participant motivation, empathic responding, and ability to work effectively as part of a multidisciplinary team.
* Strong organizational skills, including understanding of HIPAA regulations and ability to organize meetings and present reports.
* Demonstrated experience working in and fostering a diverse faculty, staff, and student environment or commitment to do so as a staff member at VCU.
Preferred Qualifications:
* Master's degree in Psychology, Neuroscience, or a related field.
* Writing experience with first-author and co-author peer-reviewed manuscripts.
* Knowledge of statistical analysis and software applications.
* Experience recruiting, consenting, and carrying out study procedures with opioid use disorder (OUD) treatment participants, including during pregnancy and postpartum.
* Qualitative research experience, including data collection, coding, analysis, and ability to set up projects and surveys in REDCap, perform sample size calculations using GPower 3.1, analyze qualitative data (such as with ATLAS.ti.8) and quantitative statistical analysis (such as with SAS 9.4 and GraphPad Prism).
* Experience with preparing and maintaining Institutional Review Board (IRB) and regulatory paperwork to comply with institutional regulatory requirements.
* Experience in mentoring and training student research trainees, incorporating them into research teams.
Job Family: Research & Innovation, University Title: Clinical Research Assistant 1, Job Code: 34001
