We are looking for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This role will support a non-interventional infectious disease clinical trial conducted at a community hospital site in Rahway, New Jersey, as part of a large pharmaceutical-sponsored study.
Requirements
- Bachelor’s degree required (healthcare, life sciences, or related field preferred)
- Minimum of one (1) year of practical experience as a Clinical Research Coordinator
- Prior experience working as a CRC in an Academic Medical Center (AMC) or community hospital setting is strongly preferred
- Phlebotomy certification or willingness to learn phlebotomy
- Experience in infectious disease studies preferred
- Strong understanding of Good Clinical Practice (GCP) and clinical trial processes
- Demonstrated ability to work independently and manage multiple priorities
- Enthusiastic and motivated team player; Self-starter with the ability to take initiative
- Excellent organizational skills and high attention to detail
- Strong interpersonal and communication skills, with a patient-centered approach
- Ability to problem-solve and adapt in a dynamic clinical environment
- Proficiency with electronic data capture (EDC) systems and Microsoft Office
Benefits
- 20 PTO days
- 9 paid holidays
- company-paid life insurance
- short- and long-term disability
- 401(k) retirement plan
- robust healthcare options