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As a Senior Administrative Assistant at ICON, you will provide high-level administrative support to executives, manage confidential information, and serve as a liaison with stakeholders. You will also assist the Regulatory Team and support special projects effectively.
As an HR Advisor, you will provide essential HR support services, addressing inquiries and offering guidance on HR processes during the employee lifecycle. Collaborate with HR Managers to resolve issues and ensure alignment with service levels, contributing to an inclusive and collaborative culture.
As a Senior Study Support Assistant at ICON plc, you will play a key role in assisting the team with study start-up tasks, administrative support, and tracking documentation. Responsibilities include submission tracking, maintaining electronic filing systems, coordinating meetings, and assisting in payment coordination. The successful candidate should have a high school diploma, good interpersonal skills, attention to detail, and English communication skills. Prior research or healthcare experience is preferred but not required.
The Clinical Research Associate II Specialist will conduct site qualifications, initiation, monitoring, and close-out visits for clinical trials. Responsibilities include ensuring protocol compliance, maintaining data integrity, collaborating with investigators, resolving data queries, and contributing to study documentation preparation.
The Set Up Specialist coordinates clinical trial start-up activities, serving as the primary contact for investigators and research coordinators. Responsibilities include adhering to ICON's values, completing the Sponsor Online Laboratory Requirements (SOLAR), managing project timelines, and serving as a resource for process improvement. Candidates should have a background in clinical trials or related areas.
As a Senior Contract Analyst, you will manage contractual agreements, ensure compliance, conduct thorough analyses of contract terms, provide guidance on contract interpretation, maintain contract records, and assist in implementing contract management processes.
The Study Start Up Associate II will lead the initiation of clinical trials by preparing and submitting regulatory documents, coordinating with stakeholders for approvals, managing regulatory records, guiding study teams, and participating in process improvements.
As a Study Start Up Associate I, you will assist in regulatory document preparation and submissions, coordinate with stakeholders to obtain necessary approvals, and maintain records. You will also support study teams in developing study documents and participate in start-up meetings focused on regulatory requirements.
The Account Executive manages client relationships, providing ongoing consultation on program strategies, budget management, and performance guarantees. Responsibilities also include client engagement, project tracking, and collaboration with internal teams to meet contract requirements and client expectations while identifying opportunities for growth.
As a Study Start Up Associate II, you will coordinate contracts and budgets with clinical sites, manage communications regarding status documents, facilitate indemnification processes, and mentor junior staff. Your role is crucial in ensuring the readiness of sites for clinical trials of new pharmaceutical and biological products.
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