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.
- Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health care
outcomes research efforts.
- Contribute to the development of medical strategies to support brand commercialization activities by working closely
management or personnel and other cross-functional management during the development of the local business plan.
Scientific Data Dissemination/Exchange
- Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines
- Understand and actively address the unsolicited scientific information needs of external health care professionals
- Support medical information associates in preparation and review of medical letters and other medical information
- Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and
Clinical Planning & Clinical Research/Trial Execution and Support
- Represent the clinical needs of the country/region to the business unit medical leadership in the development of clinical
- Review and approve local informed consent documents and risk profiles to ensure appropriate communication of risk to
- Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample
Regulatory Support Activities
- Participate in development and review of local labelling and labelling modifications in collaboration with global
- Provide medical expertise to regulatory scientists.
- Participate in advisory committees.
- Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the
- Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and
- Acts as scientific consultant and protocol expert for clinical study team members and others in medical.
- Must have completed education and training at a medical school that meets the requirements of the LiaisonCommittee on Medical Education
- Fluent in English, both verbal and written communication
- Knowledge of drug development process relevant to country/region preferred
- Strong communication, organizational and negotiation skills
- Demonstrated ability to influence others to create a positive working environment
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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