Senior Clinical Research Coordinator

Why Vitalief?

Vitalief is a trusted partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients.

We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full‑time, fully benefited Vitalief employee) to support our mission and our clients’ mission to impact and save lives.

• You can actively contribute to our clients’ mission of advancing scientific discoveries that have the potential to change patients' lives for the better.
• Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees.
• We give everyone a seat at the table – we encourage innovation.
• Life/work balance that includes 20 PTO (Paid Time Off) days plus 9 paid Holidays annually.
• Other benefits include company paid life insurance and short / long term disability coverage; 401K retirement program;
  Robust healthcare plans to choose from.

Salary Range: Market competitive - based on experience level.

Work Location: New Brunswick, NJ. Four (4) days on‑site and one (1) day remote on a weekly basis.

• Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol‑specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Phase 1 Oncology trials.
• Serves as a liaison (communicating effectively) between the organization, investigators, members of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors – to ensure that services are coordinated and delivered to patients in a timely manner.
• Maintains research record (e.g., patient consent, eligibility, Case Report Forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in Oncology trials.
• Participates in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms.
• Schedules and conducts trial visits by informing patients and coordinating procedures per protocol.
• Assesses and triages study patients appropriately for serious/unexpected adverse events (SAE), reports and records adverse events according to all applicable regulation and study protocol.
• Assists patients in understanding their diagnosis, treatment options, and the resources available including educating eligible patients about appropriate clinical research studies and technologies.

• Bachelor’s Degree required.
• Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol.
• Oncology clinical research experience is a huge plus.
• Phase 1 clinical research experience is a plus.
• Strong working knowledge of current Code of Federal Regulation and Good Clinical Practice guidelines.
• Compassionate personality and ability to interact with patients in a clear and confident manner.
• Ability to work on several trials concurrently…