Hybrid Oncology Research Regulatory Coordinator

Trinity Health; Hartford (CT); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Trinity Health Of New England seeks an Oncology Research Regulatory Coordinator to coordinate regulatory activities for clinical studies. You will support protocol submissions, prepare regulatory documents, and maintain study records to ensure compliance with policies and federal regulations.

The role is hybrid, balancing remote and onsite work as needed by the Clinical Research Manager and department requirements.

Qualifications

• Experience coordinating regulatory submissions for clinical studies.
• Familiar with ICH/GCP guidelines and applicable laws.
• Strong attention to detail and document control abilities.

Responsibilities

• Coordinate regulatory activities for clinical research studies.
• Assist with protocol submissions and regulatory document prep.
• Maintain study records to ensure compliance with policies and regulations.

Skills

Regulatory coordination

Clinical research compliance

Job description

Trinity Health Of New England seeks an Oncology Research Regulatory Coordinator to coordinate regulatory activities for clinical studies. You will support protocol submissions, prepare regulatory documents, and maintain study records to ensure compliance with policies and federal regulations.

The role is hybrid, balancing remote and onsite work as needed by the Clinical Research Manager and department requirements.