Clinical Trials Regulatory Coordinator: Impact & Compliance

Ochsner Health; Louisiana; On-site; USD 90,000 - 120,000; Full time

Job summary

Ochsner Health is seeking a Clinical Trials Coordinator to independently manage and coordinate all aspects of clinical trials in collaboration with research management and Principal Investigators. You will ensure regulatory compliance, manage data, and oversee study start-up while maintaining strong sponsor relations.

The role requires 3 years of clinical research experience or 2 years with ACRP/SOCRA certification, and a solid knowledge of research terminology and Epic.

Qualifications

• 3 years of relevant research experience in a clinical setting.
• OR 2 years of relevant research experience with Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) certification.
• Strong knowledge of medical and clinical research terminology.

Responsibilities

• Manages research activities associated with clinical trials and data management and facilitates successful study start-up.
• Maintains study compliance, ensures compliance with regulatory guidelines, and participates in internal and external audits.
• Manages data and leads special projects and tracks projects.
• Maintains strong relations with study sponsors.
• Seeks opportunities for individual and departmental continuing education.
• Performs other related duties as assigned.

Skills

Critical thinking

Clinical research terminology

Regulatory knowledge

Grant budgeting

Epic

Verbal and written communication

Organizational skills

Time management

Attention to detail

Teamwork

Education

High school diploma or equivalent

Tools

Epic

Job description

Ochsner Health is seeking a Clinical Trials Coordinator to independently manage and coordinate all aspects of clinical trials in collaboration with research management and Principal Investigators. You will ensure regulatory compliance, manage data, and oversee study start-up while maintaining strong sponsor relations.

The role requires 3 years of clinical research experience or 2 years with ACRP/SOCRA certification, and a solid knowledge of research terminology and Epic.