Regulatory Specialist - Clinical Trials & Compliance

Objective Health seeks a Regulatory Specialist to coordinate and manage regulatory research activities across sites in the United States. You will prepare, review, file, and track study-specific regulatory documents, delegate authority forms, and training logs to ensure GCP compliance and timely milestones.

Collaborating with clinical study teams and leadership, you will ensure IRB submissions, informed consent review, and audits align with FDA/ICH guidance while maintaining up-to-date regulatory

Step into the Regulatory Specialist
- Clinical Trials & Compliance role at ObjectiveGI, Inc. in United States and grow with us.

Full responsibilities and requirements are described in the listing above.

Learn more about the Regulatory Specialist
- Clinical Trials & Compliance role in the description above.

We appreciate your interest in this position.

Join ObjectiveGI, Inc. and contribute to our ongoing work.