Remote Neurology PI: Decentralized Clinical Trials

Science 37; United States; A distancia; USD 180.000 - 260.000; Jornada completa

Descripción de la vacante

Science 37, a leader in decentralized clinical trials, is seeking a Neurologist to lead and contribute as PI or Sub-Investigator on pharmaceutical-sponsored studies conducted in home-based settings. This remote role allows you to drive trial execution while maintaining patient access.

You will coordinate with Site Operations, educate the study team, engage with regulators, and help develop endpoints suitable for at-home conduct, while publishing and presenting on therapeutic area expertise.

Formación

• MD or equivalent is required.
• Board-certification in Neurology is required or equivalent.
• Experience as PI on pharm-sponsored studies is essential.
• Strong project management and leadership abilities.

Responsabilidades

• Act as Principal Investigator for studies when Science 37 executes Direct to Patient trials.
• Function as Sub-Investigator when aligned with expertise for decentralized trials.
• Coordinate with Site Operations Manager to onboard/train investigators.
• Educate/train study team on target patient population and treatment paradigms.
• Support the Commercial Team and Business Development during sponsor meetings.
• Identify fit/feasibility for decentralized trial models through study opportunity synopses/protocols.
• Regulatory engagement with FDA and other bodies on decentralized trials.
• Develop and migrate endpoints suitable for at-home conduct.

Conocimientos

PI experience

Project management

Clinical research knowledge

Communication skills

English language

Educación

MD or equivalent

Herramientas

Google applications

Descripción del empleo

Science 37, a leader in decentralized clinical trials, is seeking a Neurologist to lead and contribute as PI or Sub-Investigator on pharmaceutical-sponsored studies conducted in home-based settings. This remote role allows you to drive trial execution while maintaining patient access.

You will coordinate with Site Operations, educate the study team, engage with regulators, and help develop endpoints suitable for at-home conduct, while publishing and presenting on therapeutic area expertise.