research, including a clinical trial, and will manage research staff. The Research Coordinator will work closely with Dr. Luth to make decisions, solve problems, and identify when independent judgment should be exercised. This is a full-time position with benefits. Opportunities exist for research presentations, authorship on papers, and relevant career development activities. Candidates with an interest in behavioral health, social sciences, supportive/palliative care, and health service research are encouraged to apply. Among the key duties of this position are the following: Plans and coordinates the initiation of the research study protocol(s), and the establishment/adherence of operating policies and procedures related to research study protocols, research networks or research team. Establishes accountability for protocol assignments and study participants who are primarily older adults; demonstrates adherence to good clinical practice, and source documentation guidelines. Assesses and compiles eligibility documentation and participation status of prospective study participants and arranges baseline and follow-up appointments with potential and enrolled participants. Conducts in-person and virtual study visit as per protocol in a person-centered, clear, open-minded, non-judgmental context. Assists and develops data management systems to track study data. Assists research study operations as directed by the Principal Investigator. Minimum Education and Experience: Bachelor's degree in public health, nursing, health or social sciences, biology or related field plus three (3) years of related research experience in a health research setting required, or a master's degree plus two (2) years in a health research setting are required. Experience building project and data management systems with platforms such as RedCap and Qualtrics. Experience with qualitative data analysis including proficiency with NVivo, Dedoose and rapid analysis. Experience drafting study standard operating procedures, IRB and clinical trials.gov protocols, amendments, and continuing reviews for qualitative studies and clinical trials. Experience with regulatory reporting including drafting, formatting and inputting submissions for NIA Croms and clinical trials.gov. Experience organizing and running virtual and in-person research symposia and events. City: New Brunswick State: NJ Physical Demands and Work Environment: Physical Demands: Standing, sitting, walking, talking and hearing. No special vision requirements. Ability to lift or exert force up to 25 pounds. Work Environment: Hybrid role requiring a minimum of two in-person days per week at Family Medicine's George St. office. Additional onsite presence may be required depending on operational needs. Posting Number: 26ST1814
