Top Tech Jobs & Startups Jobs

The Data Analyst I role involves performing data analysis, ensuring quality assurance, and formatting data according to specifications. Responsibilities include data reconciliation, forecasting, quality checks of imaging and cardiac data, and training team members. The role necessitates a life-science background and experience in the data analyst field.

The role involves supporting investigator recruitment, managing timelines, maintaining data accuracy, and serving as the primary contact for clinical trial sites. Responsibilities include conducting remote site management activities, contacting clinical sites for updates, participating in QA audits, and ensuring sponsor and patient confidentiality.

The Study Start Up Associate II will lead the preparation and submission of regulatory documents for clinical trials, manage approvals with stakeholders, maintain accurate records of submissions, and support the study teams with regulatory guidelines and process improvements.

As a Contract Analyst II, you will review and analyze contracts related to clinical trials, negotiate terms with clients and vendors, collaborate with teams to assess risks and improve contracts, maintain records of contract status, and provide support on contract-related issues.

The Clinical Trial Administrator supports coordination and administration of clinical trials, ensuring compliance with protocols, maintaining documentation, preparing study materials, and tracking trial metrics. This role facilitates communication across teams for smooth trial execution and contributes to the advancement of innovative therapies.

As a Study Start Up Associate I, you will conduct feasibility studies, site identification, and contract negotiations related to clinical research. You'll provide country-specific expertise to the Study Start Up team, manage submissions to regulatory bodies, and ensure proper documentation such as informed consent forms are prepared accurately.

As a Clinical Research Associate at ICON, you will manage the setup, monitoring, and close-out of clinical studies, ensuring compliance with regulations and ICH-GCP principles. You will handle submissions, respond to inquiries, and contribute to training fellow CRAs.