Director - Clinical Research Scientist - Global and US Medical Affairs

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first.

We’re looking for people who are determined to make life better for people around the world.

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

The Clinical Research Scientist (CRS) within the Business Unit – Medical Affairs provides scientific and clinical expertise to support product strategy and execute medical plan tactics, customer engagement, and evidence generation. This role ensures that medical insights, clinical data, and regulatory considerations are effectively integrated into local business activities and global development plans.

• Anticipate and respond to scientific and clinical information needs from healthcare providers, payers, and patient groups.
• Lead data analyses and health outcomes research to address customer questions.
• Contribute to medical strategy and brand planning in collaboration with global Medical Affairs, GPO/RWE, PRA, and commercial partners.
• Provide medical expertise for payer partnerships, promotional material review, and business‑to‑business/government engagements.
• Support training of sales, medical, and patient support teams.
• Lead definition of Patient Journey and contribute clinical perspective to patient programs.
• Participate in relevant professional and industry associations.

• Ensure compliance with global and local regulations governing scientific communication.
• Address unsolicited scientific inquiries in alignment with medical governance standards.
• Support scientific meetings, advisory boards, symposia, and other expert engagements.
• Prepare or review medical letters, slide decks, abstracts, posters, and manuscripts.
• Build and maintain relationships with key opinion leaders and scientific societies.
• Represent the company at medical congresses and support scientific booth activities.
• Contribute to data analyses, publication development, and Clinical Trial Registry reporting.

• Align clinical strategies with regional needs by collaborating with Medical Affairs and global development teams.
• Communicate local research needs to ensure Phase I–IV programs reflect market and customer requirements.
• Maintain up‑to‑date understanding of clinical and competitive data.
• Provide regional clinical insights to inform development plans and study protocols.

• Review and approve informed consent documents to ensure accurate risk communication.
• Partner with clinical operations, statisticians, and investigators throughout study design, initiation, conduct, and close‑out.
• Support investigator/site training and address study‑related medical questions.
• Oversee local safety monitoring and adverse event follow‑up.
• Review investigator‑initiated trial (IIT) proposals as needed.
• Ensure global alignment of Phase 3b/4 and applicable early‑phase studies.

• Contribute to development and review of local labeling and labeling changes.
• Provide medical input for regulatory submissions, advisory committee preparation, and local registration activities.
• Participate in risk management planning with global and local teams.

• Stay informed on therapeutic area trends, market changes, and competitive landscape.
• Provide scientific training to clinical study teams and act as a protocol subject‑matter expert.
• Represent the…