This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Navigator I based in India.

We are seeking a detail-oriented Site Navigator I to coordinate clinical trial site activities and support the successful start-up and activation of research sites. In this role, you will serve as a primary point of contact for investigative sites, facilitating communication between clinical teams, sponsors, CROs, and regulatory stakeholders. You will oversee site feasibility, initial outreach, essential documentation, regulatory submissions, and activation milestones to ensure studies progress efficiently. Working within established clinical research standards, you will help maintain compliance with ICH/GCP guidelines, local regulations, and study-specific requirements. You will also support site contracts, budgets, training, and ongoing documentation management while proactively identifying risks that could affect study timelines. This remote chance is ideal for an organized professional who values patient safety,



operational excellence, and collaboration in a regulated clinical research environment.
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Accountabilities

• Site Identification and Feasibility: Identify potential investigative sites that meet study requirements, assess their capabilities and resources, conduct initial outreach, obtain confidentiality agreements, and coordinate feasibility questionnaires.

• Site Start-Up and Activation: Coordinate site-level start-up activities from feasibility through activation, tracking milestones, deadlines, submissions, and outstanding requirements to ensure timely study initiation.

• Regulatory Compliance and Documentation: Collect, review, track, and maintain essential site documents in accordance with ICH/GCP guidelines, applicable regulations, standard operating procedures, and study-specific requirements.

• Pre-Study Visits: Coordinate remote pre-study visits, including preparation, foll

📌 Site Navigator I (India)
🏢 Jobgether
📍 India