- Experiencia
- Cualquier
- Salario
- —
- Vacantes
- 1
- Al corriente
- Hace 2 horas
- Modo de trabajo
- Trabajar desde casa
- Reanudar
- Se requiere solicitud
Descripción del trabajo
Overview
Join Alignerr as a Clinical Study Manager contributing your clinical trial expertise to help develop advanced AI models informed by genuine healthcare research data. This role allows you to oversee the execution of clinical trials remotely, managing complex projects with multiple vendors and partners.
Key Responsibilities
- Control clinical trial timelines, milestones, and deliverables to ensure projects progress according to schedule from initiation through completion.
- Manage study budgets, including forecasting and monitoring costs across various external vendors and stakeholders.
- Coordinate activities among Contract Research Organizations (CROs), investigative sites, and internal teams to guarantee seamless and high-quality trial execution.
- Proactively identify operational risks, address challenges early, and keep all parties aligned throughout the clinical trial lifecycle.
- Leverage your substantial clinical knowledge in AI training tasks requiring deep domain insight and sound judgment.
Candidate Profile
- Demonstrated experience as a clinical trial project manager with proficiency in managing budgets, timelines, and clinical operations.
- Proven ability to oversee CROs, external vendors, or research partners within regulated environments.
- Adept at multitasking multiple workstreams and ensuring smooth operations in complex, cross-functional clinical studies.
- Meticulous, well-organized, and confident in making decisions under pressure.
- Comfortable working autonomously and asynchronously in a fully remote setting.
Preferred Qualifications
- Experience related to data annotation, evaluating data quality, or involvement in AI training workflows.
- Knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and regulatory submission procedures.
- Therapeutic area expertise, especially in oncology, rare diseases, or other complex trial types.
- Familiarity with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) systems, or other clinical operations platforms.
Why Work With Us
- Engage in cutting-edge AI initiatives alongside leading global research laboratories.
- Enjoy full remote work flexibility, allowing you to set your own schedule and work location.
- Experience the independence of contract work combined with impactful responsibilities.
- Use your professional knowledge to influence how AI interprets and understands clinical research data.
- Opportunity for contract extension and continued collaboration on new projects.
- Join a worldwide network of experts from healthcare, scientific research, and technology sectors.