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Clinical Research Coordinator Ii (Multiple Vacancies)
Company | Rutgers University |
Address | New Brunswick, NJ, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-08-27 |
Posted at | 9 months ago |
Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply for this Job link/button.
- Perform administrative tasks for the clinical research department including filing, appointment scheduling, phone follow ups, mailings, supply inventory, investigational product inventory etc.
- Screen patients to identify eligible study candidates through chart review, patient interviews, discussions with practice doctors, and other methods.
- Explain studies to eligible candidates, answer questions, and obtain written consent as delegated by the study PI and/or Research Director.
- Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines.
- Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
- Facilitate enrollment of eligible patients by working closely with physicians and staff.
- The candidate must possess a Bachelor’s Degree in relevant field plus 2 years of clinical research experience as a Clinical Research Coordinator, with expertise in patient recruitment, pre-screening, consenting, retention, activation, regulatory compliance, and data management.
- This role requires strong organizational and prioritization skills, as the coordinator will be responsible for managing 4 to 5 concurrent trials.
- Excellent interpersonal skills are essential for clear and confident patient interactions.
- The coordinator must also collaborate effectively with physicians, nurses, hospital staff, and laboratory personnel to ensure the timely and coordinated delivery of services to patients.
- The keys to success in this role are versatility, a positive “can do” attitude, and adaptability.
- The ability to make independent decisions and thrive in a fast-paced environment while managing multiple concurrent trials is crucial. Proficiency in Microsoft Office is required, and familiarity with EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is advantageous.
- A thorough understanding of Good Clinical Practice ( GCP ) guidelines is necessary, along with experience in preparing documents for submission to the Institutional Review Board ( IRB ) and reporting Serious Adverse Events (SAEs) within specified deadlines.
- Experience in cardiology and complex clinical trials is a plus.
- Work Environment: Laboratory environment. Moderate noise
- Physical Demands: Standing, sitting, walking, talking or hearing. No special vision requirements. Lifting (up to 25 pounds).
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