Senior Clinical Research Physician — Cardiometabolic

Regulatory Jobs; Indianapolis (IN); Híbrido; USD 201.000 - 394.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Company bonus

401(k) plan

Medical/dental/vision benefits

Descripción de la vacante

Lilly in Indianapolis is seeking a Clinical Research Physician for the Cardiometabolic Research (CMR) Program. The role focuses on early-phase compound development, global trial execution, regulatory support, and scientific data dissemination.

Collaboration with local and international investigators, pharmacology and PK/PD teams is essential to optimize study design and patient outcomes. You will oversee Phase I–IIb studies, design protocols, monitor safety, and contribute to strategic trial

Formación

• Must be Medical Doctor or Doctor of Osteopathy and board eligible/certified.
• US-trained physicians must have board eligibility or certification.
• Non-US trained physicians must have LCME-equivalent education and training.
• Fluent in English; strong written and verbal communication.
• Willing to travel domestically and internationally as required.

Responsabilidades

• Design and oversee Phase I–IIb clinical studies and contribute to phase planning.
• Write and review clinical trial protocols and development plans.
• Collaborate with investigators, consultants and staff globally on protocols and data collection.
• Monitor patient safety and adverse events per corporate safety policies.
• Support regulatory reporting, labeling discussions and dissemination of results.
• Lead and participate in scientific communications, publications and congress activities.

Conocimientos

Fluent English

Interpersonal skills

Organizational skills

Negotiation skills

Teamwork

Willing to travel

Educación

MD or DO

Board eligibility/certification

Descripción del empleo

Lilly in Indianapolis is seeking a Clinical Research Physician for the Cardiometabolic Research (CMR) Program. The role focuses on early-phase compound development, global trial execution, regulatory support, and scientific data dissemination.

Collaboration with local and international investigators, pharmacology and PK/PD teams is essential to optimize study design and patient outcomes. You will oversee Phase I–IIb studies, design protocols, monitor safety, and contribute to strategic trial