The Senior Clinical Research Associate (Sr. CRA) is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. The Sr.CRA works closely to ensure that study commitments are achieved efficiently.

The Genetics Lead oversees genetics programs, operations, and quality metrics, playing an integral role in collaborating with the broader clinical team, product, operations, and all other teams across the organization. This is a contract 1099 role with 10-20 hrs needed per week involving maintain clinical protocols,report and letter templates for documenting patient consults, and clinical forms

Tackle complex, high-impact problems in medical billing and health insurance. Continuously learn about healthcare, insurance regulations, and patient advocacy. Directly support patients by resolving cases related to billing, benefits, insurance challenges & much more! Shape operations & product in a fast-moving early-stage environment.

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials, supporting the completion and coordination of logistical and administrative tasks. Responsibilities include data collection for regulatory submissions, document tracking, managing the delivery of study supplies, and maintaining relationships with site staff.

The Global CTA performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities. Tasks include essential document collection, site recruitment, regulatory submissions and clinical data review, while maintaining study documentation in applicable systems.

Join a great team where our residents and patients are at the heart of everything we do! You'll provide compassionate care to skilled nursing and/or rehab residents, consistently meet DOH/state/federal and company standards and serve as an active member of the interdisciplinary team. You will also support the food service operation as needed.

This role involves supporting children with speech, language, and communication difficulties through assessment and therapy. The successful candidate will play a vital role in enhancing the communication abilities and overall development of children in their care. The Remote Speech and Language Therapist will be responsible for conducting assessments, developing and implementing therapy plans, and monitoring progress.

Manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files, ensuring data quality, compliance with SOPs, regulatory requirements, and study completion on time and within budget.

As Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence, dedicated to one of our global pharmaceutical clients, with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. You will have full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.

This is a remote role responsible for processing medical record requests by taking calls from patients, insurance companies and attorneys to provide medical record status and documenting information in multiple platforms using two computer monitors in a high-volume production environment. Proficient in Microsoft office (including Word and Excel) is needed.