Eli Lilly and Company, a global healthcare leader based in Indianapolis, Indiana, is committed to making life better for people worldwide. With a legacy of pioneering innovations, Lilly prioritizes compassion and cutting-edge research. The company emphasizes not only delivering life-changing medicines but also fostering a supportive work environment where employees are empowered to excel. With a strong foundation in philanthropy and volunteerism, Lilly creates a workplace where people strive to make a positive impact both in their careers and communities.
Role Overview: Quality-Medical Affairs Professional (Q-MAP)
As a Quality-Medical Affairs Professional (Q-MAP) at Lilly, you will be a vital contributor to the medical affairs division, ensuring that both promotional and non-promotional materials meet the highest standards of quality, accuracy, and compliance. This role requires a combination of scientific expertise, strategic thinking, and collaborative abilities to uphold the integrity and effectiveness of communications.
Key Responsibilities
Brand Team Support
- Act as a primary medical liaison for the brand team.
- Provide clinical and scientific insights to cross-functional teams.
- Participate in the development and review of promotional and medical materials.
- Assist in the creation of local brand plans and medical strategies.
- Share in-depth therapeutic knowledge and up-to-date medical insights.
- Support the medical training of internal stakeholders.
Scientific Expertise and Medical Affairs Delivery
- Assist with data analysis and the preparation of scientific publications, including abstracts, posters, and manuscripts.
- Collaborate with various medical affairs roles (e.g., Clinical Research Physicians, Clinical Research Scientists, Medical Science Liaisons) for cohesive team operations.
- Contribute scientifically to the development and review of content.
- Stay current with medical literature and trends in the therapeutic area.
- Develop a robust understanding of clinical practice projections and patient access concerns.
Qualifications
Minimum Requirements
- Advanced Degree: MD, PhD, or equivalent in health sciences with a minimum of 2 years of clinical or therapeutic experience.
- Alternative Qualifications: Bachelor’s or Master’s degree (e.g., MBBS, BDS, PharmD, MSc Nursing) with 2+ years of relevant clinical experience.
Skills and Competencies
- Strong interpersonal and communication abilities.
- Experience working in cross-functional teams, with capabilities in project management.
- Proven expertise in translating scientific data into clear, impactful content.
- An understanding of compliance, regulatory standards, and medical ethics.
- Ability to manage complex projects and prioritize tasks effectively.
- Experience interfacing with customers and influencing key decision-makers.
