Clinical Research Coordinator: Lead Trial Operations

Tandem Intermediate LLC; Somers Point (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

Tandem Intermediate LLC in New Jersey seeks aClinical Research Coordinator to oversee daily operations of clinical studies, coordinating with investigators, sponsors, and CROs to ensure protocol compliance and ethical standards.

You will own study coordination, documentation, data management, and sponsor communication from start-up to close-out, while supporting recruitment, informed consent, safety reporting, and data entry in a multidisciplinary team.

Qualifications

• Bachelor's degree in a related field
• Minimum of two (2) years of clinical research or clinical trial management experience
• Medical certification or licensure preferred (e.g., MS, LPN, RN)
• Phlebotomy: prior experience performing blood draws and handling biological specimens required

Responsibilities

• Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out
• Support start-up activities including feasibility, regulatory submissions, and site activation
• Attend investigator meetings and site initiation visits
• Manage visit schedules and coordinate study-related activities across clinical teams
• Collaborate with recruitment teams to support participant screening and enrollment
• Conduct informed consent discussions with participants and document consent
• Monitor study subjects and report adverse events in collaboration with PI and staff
• Enter study data into EDC and other required systems
• Complete, verify, and resolve case report forms and sponsor/monitor queries
• Report protocol deviations to PI, sponsor, and IRB

Skills

Leadership

Communication

Organizational skills

Attention to detail

Regulatory compliance

Independent & collaborative

Time management

Proficiency with office equipment

Confidentiality

Education

Bachelor's degree

Tools

EDC systems

Job description

Tandem Intermediate LLC in New Jersey seeks aClinical Research Coordinator to oversee daily operations of clinical studies, coordinating with investigators, sponsors, and CROs to ensure protocol compliance and ethical standards.

You will own study coordination, documentation, data management, and sponsor communication from start-up to close-out, while supporting recruitment, informed consent, safety reporting, and data entry in a multidisciplinary team.