Clinical Research Coordinator

ABOUT VITALIEF

Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to academic medical centers, health systems, sponsors, CROs, and site networks. By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients.

We are seeking an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full‑time employee with comprehensive benefits. This position will support a long‑term observational vascular medical device registry study at a community hospital site in Newark, NJ. The ideal candidate will have a minimum of two years of CRC experience, exceptional attention to detail, a strong interest in cardiovascular research, and the ability to work independently while serving as the primary coordinator for the study.

• Manage day‑to‑day study activities as the primary site coordinator, working directly with the PI.
• Identify, screen, consent, enroll, and follow‑up with study participants and maintain accurate source documentation.

• Review participant records in EPIC to support study requirements and clinical data collection.
• Complete case report forms (eCRFs), perform data entry, and resolve data queries.
• Ensure accuracy, completeness, and compliance of study documentation.

• Maintain essential regulatory documents, including investigator files, training records, licenses, and delegation logs.
• Support IRB submissions, continuing reviews, amendments, and regulatory correspondence.
• Ensure ongoing compliance with protocol requirements, GCP, and research standards.

• Serve as a primary contact for sponsors, CROs, IRBs, and internal research teams.
• Support monitoring visits, site meetings, issue resolution, maintain study readiness and study closeout activities.

• Assist with clinical trial agreement (CTA) coordination and budget‑related activities.
• Collaborate with legal, finance, and sponsor teams to support study operations.

• Bachelor's degree in health science, life science, nursing, or related field.
• Minimum 2 years of clinical research coordination experience, including device, registry, or observational trials; interventional experience a plus.
• Experience managing regulatory documentation, IRB submissions, informed consent processes, and participant interaction.
• Proficiency with EPIC (preferred), Microsoft Office, and clinical research databases/CTMS systems.
• Ability to work effectively as the primary coordinator at a research site with limited day‑to‑day oversight.
• Strong organizational skills with the ability to independently prioritize and manage multiple responsibilities.
• Sharp attention to detail and commitment to research compliance and data quality.
• Self‑starter who thrives with minimal oversight, communicates effectively across leadership, investigators, sponsors, and cross‑functional teams, and proactively resolves issues.

• Impactful Work:
  Contribute to scientific advancements that directly improve patient lives in the field of cardiovascular medicine.
• People‑First Culture:
  Thrive in an environment that fosters growth, innovation, and collaboration.
• Comprehensive Benefits: 20 PTO days, 9 paid holidays, company‑paid life insurance, short‑ and long‑term disability, a 401(k) retirement plan, and robust healthcare options.
• Work Location:
  
  Hybrid 2‑3 days per week onsite in Newark, NJ, with flexibility for remote work on remaining days.
• Salary Range: $65,000 to $78,000 (depending on experience level).

Standing, sitting, walking, visual perception, talking and hearing.

Vitalief partners with clients such as major medical centers and academic institutions that often require all on‑site resources such as prospective Vitalief consultants to be inoculated annually for influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium tuberculosis.