Clinical Trial Assistant

Step into the world of clinical research with Excelya as a Clinical Trial Assistant. This role offers you a unique opportunity to be involved in the critical processes of clinical trials while collaborating with a team that is dedicated to making a difference.

Requirements

• Assist in the operational management of clinical trials under the guidance of Clinical Project Managers and CRAs.
• Ensure the Trial Master File (TMF) is maintained and updated, adhering to GCP and regulatory standards.
• Support the preparation and review of essential clinical documents, including study protocols and patient consent forms.
• Coordinate logistics for study supplies and materials, ensuring timely delivery to clinical sites.
• Utilize clinical management systems to monitor study progress and track key metrics.
• Organize meetings and documents, preparing agendas, minutes, and follow-up activities as required.
• Act as a point of contact for clinical trial sites, assisting with queries and document requests.
• Support site initiation and close-out visits, ensuring all regulatory requirements are met.
• Manage administrative tasks related to study budgets, contracts, and vendor relations.
• Maintain compliance and audit readiness of all clinical documentation throughout the trial lifecycle.

Benefits

• Competitive salary
• Generous benefits package
• Opportunities for career growth and development
• Collaborative and dynamic work environment