Clinical Trials Coordinator & Data Steward

Tandem Intermediate LLC; Stonehurst West (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

Tandem Intermediate LLC in New Jersey is seeking a Clinical Research Coordinator to oversee daily operational activities of assigned clinical studies. You will work with investigators, staff, sponsors, and CROs to ensure studies comply with protocols, regulations, and ethical standards.

Responsibilities include study management, participant recruitment and consent, data entry, QA, phlebotomy (when trained), and sponsor communications, with a focus on accuracy, documentation, and timely reporting.

Qualifications

• Bachelor’s degree in a related field is required.
• Minimum of two years of clinical research or trial management experience.
• Medical certification or licensure (e.g., MS, LPN, RN) preferred.
• Phlebotomy experience is required where trained

Responsibilities

• Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
• Support startup activities including feasibility, regulatory submissions, and site activation.
• Attend investigator meetings and site initiation visits.
• Manage visit schedules and coordinate study activities across clinical teams.
• Collaborate on participant screening, enrollment, and informed consent discussions.
• Monitor subjects and report adverse events in collaboration with the PI and staff.

Skills

Leadership

Communication

Organization

Regulatory compliance

Attention to detail

Education

Bachelor’s degree in related field

Medical certification/licensure preferred

Tools

EDC systems

Job description

Tandem Intermediate LLC in New Jersey is seeking a Clinical Research Coordinator to oversee daily operational activities of assigned clinical studies. You will work with investigators, staff, sponsors, and CROs to ensure studies comply with protocols, regulations, and ethical standards.

Responsibilities include study management, participant recruitment and consent, data entry, QA, phlebotomy (when trained), and sponsor communications, with a focus on accuracy, documentation, and timely reporting.