Clinical Trials Coordinator: Study Ops, Data & Compliance

Tandem Intermediate LLC; Marrero (LA); On-site; USD 55,000 - 75,000; Full time

Job summary

Tandem Intermediate LLC is seeking a Clinical Research Coordinator to oversee daily operations of assigned clinical trials. You will work with investigators, sponsors, and CROs to ensure studies comply with protocols, regulatory requirements, and ethical standards.

Key duties include study start-up, participant recruitment, informed consent, data entry in EDC, and sponsor communications, while maintaining source documentation and trial records in good order.

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.
• Phlebotomy experience required.

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.

Skills

Leadership

Communication

Regulatory compliance

Documentation

Data management

Multitasking

Education

Bachelor's degree

Tools

EDC

Job description

Tandem Intermediate LLC is seeking a Clinical Research Coordinator to oversee daily operations of assigned clinical trials. You will work with investigators, sponsors, and CROs to ensure studies comply with protocols, regulatory requirements, and ethical standards.

Key duties include study start-up, participant recruitment, informed consent, data entry in EDC, and sponsor communications, while maintaining source documentation and trial records in good order.