Senior Clinical Research Coordinator Lead
3 days ago
Vitalief is a leading site solutions partner focused on improving the value and contribution of clinical trial sites and research projects across large multi-center grants. Our company values people-first culture, prioritizing personal and professional growth for all employees.
About the Role
This is an exciting opportunity to join our exceptional client team as a Lead Clinical Research Coordinator (full-time, fully benefited Vitalief employee) supporting a groundbreaking research surgery pilot project. You will work closely with our team, client's CRC team, and play a key role in preparing for a future clinical trial. This innovative project offers hands-on experience in a first-of-its-kind study.
Responsibilities
- Perform protocol-specific tasks including surgical patient screening, informed consent, protocol required imaging, study follow-up, and data entry.
- Evaluate processes and recommend Standard Operating Procedures improvements, including optimal data collection methods.
- Follow and maintain a processing and tracking system for enrolled study patients and protocol related processes.
- Coordinate with surgeons to review elective cases, emergent cases, and be available for unanticipated trauma cases.
- Educate participants on technology used and assist with troubleshooting.
- Track and submit adverse events per site protocol.
Requirements
- Bachelor's Degree required; Master's degree preferred, ideally in healthcare.
- Minimum 2 years of experience in clinical research as a Senior/Lead Clinical Research Coordinator.
- Strong working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines.
- Ability to analyze and recommend clinical research SOPs improvements.
- 20 PTO days plus 9 paid Holidays annually.
- Company-paid life insurance and short/long-term disability coverage.
- 401K retirement program.
- Robust healthcare plans.
Location:New Brunswick, NJ.
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