Research Associate at Trinity Health · Saint…

Summary: Trinity Health is a healthcare organization seeking a Research Associate to assist in coordinating clinical research studies. The role involves recruiting patients, obtaining informed consent, and managing research data to ensure compliance with established protocols and guidelines. Responsibilities: - Monitor obstetrical clinic schedules to screen for potential participants - Review the medical record to assess eligibility based on defined criteria - Recruit patients and obtain informed consent to Mission and Department standards. Consenting process includes the ability to do phone calls, e-consent, or in-person - Conduct research surveys and other protocol activities - Enter, clean, and manage research data - Organize study supplies and request inventory as needed - Reviews the accuracy, completeness, and timeliness of completed study related records, case report forms, and other documents - Learn and adhere to clinic visitor, infection control, contact policies and appropriate provider communication - Communicate questions and findings in a timely manner to the appropriate parties beginning with the Research Coordinator and possibly including but not limited to research administration, principal investigators, and compliance staff - Assist in the preparation of IRB reports and submissions - Assist with non-invasive study procedures with prior IRB approval (minimal risk studies only) upon completion of orientation requirements under direct supervision of a Research Coordinator - Perform clerical duties, schedule meetings - Performs related responsibilities, and special projects as required Required Qualifications: - Bachelor's degree in a related science, healthcare or business field or the equivalent combination of education and experience - One year of related research experience preferred - Familiarity with the principles of obtaining informed consent preferred - Knowledge of basic research design principles, statistics, regulatory and ethical requirements preferred - Knowledge of medical terminology preferred - Excellent writing and interpersonal communication skills - Working knowledge of database systems and good basic computer skills - Ability to work some flexible hours to accommodate study and patient schedules is required - Ability to work independently and with high accountability, and ability to work in team settings Preferred Qualifications: - One year of related research experience preferred - Familiarity with the principles of obtaining informed consent preferred - Knowledge of basic research design principles, statistics, regulatory and ethical requirements preferred - Knowledge of medical terminology preferred Required Skills: Informed consent, Research design principles, Statistics, Regulatory and ethical requirements, Medical terminology, Database systems, Research data management Benefits: Competitive compensation, DAILYPAY, Benefits effective Day One! No waiting periods., Full benefits package including Medical, Dental, Vision, PTO, Life Insurance, Short and Long-term Disability, Retirement savings plan with employer match and contributions, Opportunity for growth and advancement throughout Trinity Health, Tuition Reimbursement