Position Details
- Demonstrates competence in utilizing computerized systems as required (Sunrise Disease/Clinical Manager, Oncore™, IDX, TDS, Medical Records database, etc.). Demonstrates basic knowledge to accomplish core tasks (SAE completion, access protocol attachments via Oncore™, enter charts into Medical Records Database, format and print patient study calendars, etc.).
- Attends Training Programs, Modules, workshop, and seminars sponsored by OHRS as applicable; Actively participates in disease specific DSG meetings; quality assurance activities such as audits and meetings with the Principal Investigator, when directed by supervisor, to keep up-to-date on departmental objectives. Participates in task-forces and/or committees as applicable and/or other process improvement initiatives as assigned.
- Assists with training, orientation, and precepting new staff members.
- Ensures that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board and followed as written.
- Maintains up-to-date knowledge and adheres to policies, procedures, guidance, and practice standards set forth by RBHS, Cancer Institute of New Jersey, FDA, and all regulatory bodies. Documents and maintains mandatory RBHS employee requirements such as Blood Borne Pathogens, Right-to-Know, Tuberculosis, Hand-Washing, as defined by Environmental & Occupational Health & Safety Services (EOHSS), Joint Commission on the Accreditation of Healthcare Organizations (JCAHO) and other institutional requirements.
Rutgers also offers a benefit program to eligible full-time postdoctoral fellow students. For details, please go to https://finance.rutgers.edu/healthcare-risk/insurance/postdoctoral-health-insurance.
- Bachelor’s Degree in a social science or related field is required.
- Equivalent education, experience and/or training may be substituted for the educational requirement.
- Minimum of three (3) years of clinical research experience required.
- The ideal candidate will be detail oriented, have excellent organizational skills, be proficient in computer applications (Word, Excel, Oncore™), possess excellent communication and interpersonal skills, be able to maximize resources and be resourceful.
- Nursing degree preferred.
- Bilingual skills (English/Spanish); speaking, reading, and writing preferred.
- At least one (1) year of oncology experience preferred.
- Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred.
WORK ENVIRONMENT: Office environment. Moderate noise.