Clinical Research Coordinator: Drive Trials and Compliance

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

Job summary

Tandem Intermediate LLC is seeking a Clinical Research Coordinator (CRC) to oversee and manage the daily operational activities of assigned clinical research studies. This role works with investigators, clinical staff, participants, sponsors, and CROs to ensure that all research activities comply with study protocols and regulatory standards.

The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution

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 (e.g., MS, LPN, RN) preferred

Responsibilities

• Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
• Support study start-up activities including feasibility, regulatory submissions, and site activation.
• Attend investigator meetings, site initiation visits, and other study-related meetings.
• 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 and report adverse events in collaboration with the PI and clinical staff.
• Maintain accurate source documentation, CRFs, regulatory files, and study records.
• Enter study data into EDC and other required systems; resolve queries.
• Ensure SOPs, GCP, and regulatory compliance; maintain confidentiality.

Job description

Tandem Intermediate LLC is seeking a Clinical Research Coordinator (CRC) to oversee and manage the daily operational activities of assigned clinical research studies. This role works with investigators, clinical staff, participants, sponsors, and CROs to ensure that all research activities comply with study protocols and regulatory standards.

The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution