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As a Clinical Research Associate II, you will manage clinical trials, ensure compliance, analyze data, and support study documentation.

The Senior Site Specialist manages clinical trial start-up processes, including contract negotiation, site connection, and training new staff. Responsibilities include reviewing contracts, facilitating indemnification processes, and acting as a consultant on budgets.

As an IHCRA, you will assist in planning and executing clinical trials, ensure compliance with protocols, and monitor study progress.

The In-House CRA will support and manage clinical trials, conduct site assessments, ensure compliance, and monitor study progress.

As an IHCRA, you will support the execution and management of clinical trials, conduct site assessments, ensure compliance, and monitor study progress.