Research Assistant, Population Sciences - Department of Oncology

Wayne State University•Detroit, MI

7d•Onsite

About The Position

Wayne State University is searching for an experienced Research Assistant, Population Sciences - Department of Oncology at its Detroit campus location. Wayne State is a premier, public, urban research university located in the heart of Detroit, Michigan where students from all backgrounds are offered a rich, high-quality education. Our deep-rooted commitment to excellence, collaboration, integrity, diversity and inclusion creates exceptional educational opportunities which prepare students for success in a global society.

Requirements

Bachelor's degree in a related field of study.
Requires advanced knowledge predominantly intellectual in character in a field of science or learning acquired by a prolonged course of specialized intellectual instruction.
Ability to work independently and manage multiple clinical research activities while adhering to study protocols, regulatory requirements, and timelines.
Ability to analyze, summarize, and interpret clinical research data and communicate findings effectively in reports and presentations.
Requires knowledge predominantly intellectual in character in a field of science or learning acquired through specialized instruction.
Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards).
Excellent time management, organizational, and documentation skills.
Strong interpersonal and communication skills, with demonstrated ability to interact professionally with research participants, clinical staff, and multidisciplinary research teams.
Ability to recruit and communicate effectively with diverse populations, including medically underserved communities.

Nice To Haves

Experience conducting clinical or human subject research is preferred.
Experience with participant recruitment, informed consent, data collection, and maintenance of regulatory documentation is preferred.
Proficiency in Microsoft Office software (Word, Excel, PowerPoint) and familiarity with clinical research databases or electronic data capture systems is preferred.
Bachelor’s degree from an accredited college or university in public health, psychology, social sciences, nursing, biology, or related field.

Responsibilities

Support the design and implementation of clinical research protocols involving human subjects.
Recruit and screen study participants through approved methods, including outreach, surveys, and interviews.
Conduct study visits and collect clinical and research data in compliance with Institutional Review Board (IRB), regulatory, and protocol requirements.
Communicate regularly with the Principal Investigator and research team regarding study progress and participant status.
Collect, enter, and maintain accurate clinical and research data, including outcomes, surveys, and case report forms.
Monitor data quality and completeness.
Perform preliminary data analysis and generate graphs, charts, and tables to summarize results in accordance with study protocols.
Proofread and verify research data and documentation for accuracy.
Prepare and assist with presentations of research findings for professional, scientific, and academic conferences.
Organize and summarize study results for submission to peer-reviewed journals.
Assist in drafting, factchecking, editing, and proofreading scientific manuscripts, study reports, and regulatory documents.
Maintain organized research records and study files in accordance with regulatory and institutional requirements.
Coordinate study materials and supplies, and support documentation for audits, monitoring visits, and regulatory submissions.
Ensure workspaces remain organized and compliant with confidentiality and data security standards.
Setting up and running video and audio recording equipment in the exam room in adherence to IRB guidelines
Perform other related duties as assigned.