Research Program Manager (Statewide)

Rutgers University; New Brunswick (NJ); Vor Ort; USD 106.000 - 162.000; Vollzeit

Zusammenfassung

Rutgers University is hiring a Research Program Manager (Statewide) to establish workflows and processes that support clinical research across the Rutgers Oncology service line, supervise staff, ensure regulatory compliance, and liaise between local sites and the Office of Human Research Services.

The role requires a Bachelor's degree in a social science or related field, five years of oncology research experience, two years of supervisory experience, and BLS certification; nursing degree or

Qualifikationen

• Bachelor’s degree in a social science or related field.
• At least five years of oncology research experience.
• At least two years of supervisory experience.
• Proficiency with Word, Excel, and Oncore.
• BLS certification required; nursing degree and clinical research certification preferred; bilingual skills a plus.

Aufgaben

• Supervise daily statewide clinical research operations and serve as primary contact for protocol-related requests.
• Provide support and conduct performance evaluations for research staff.
• Create a patient-centered environment, collaborating with physicians and interdisciplinary teams.
• Perform data abstraction from clinical records, publications, and external physician offices.
• Plan and facilitate staff training and in-service meetings.
• Conduct QA audits to ensure data accuracy and compliance with protocols.
• Work collaboratively with clinical and research personnel including nurses, pharmacy, reception, and hospital staff.

Kenntnisse

Staff supervision

Clinical research coordination

Data abstraction

Quality assurance

Word

Excel

Oncore

Ausbildung

Bachelor's degree in social science or related field

Tools

Oncore

Jobbeschreibung

Rutgers University is hiring a Research Program Manager (Statewide). The role involves establishing workflows and processes to support clinical research across the Rutgers Oncology service line, supervising research staff, ensuring compliance with Good Clinical Practice and regulatory guidelines, and acting as a liaison between local sites and the Office of Human Research Services.

Highlights

• Supervise daily statewide clinical research operations and serve as primary contact for protocol-related requests.
• Provide support and conduct performance evaluations for research staff, identifying strengths and improvement areas.
• Create a patient-centered environment, collaborating closely with physicians and interdisciplinary teams.
• Perform data abstraction from clinical records, publications, and external physician offices.
• Plan and facilitate staff training and in-service meetings to maintain research skills.
• Conduct Quality Assurance audits to ensure data accuracy and compliance with protocols.
• Work collaboratively with clinical and research personnel including nurses, pharmacy, reception, and hospital staff.
• Require proficiency with computer applications, including Word, Excel, and Oncore™ clinical trial management system.
• Must have a Bachelor's degree in a social science or related field, five years of oncology research experience, and two years of supervisory experience.
• American Heart Association Basic Life Support (BLS) certification required; preferred qualifications include nursing degree, union supervision experience, clinical research certification, and bilingual skills.
• Salary range from $105,763 to $161,814 annually, with a full-time 37.5-hour workweek and on-site work arrangement.