(Sr) Associate- MI

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.

Purpose:

The purpose of the Medical Information Associate/Sr. Associate role in Korea is to provide external customers and internal employees with balanced scientific information in response to their unsolicited requests and to review promotional materials according to local regulations, SOPs, mandatory requirements, and guidelines.

Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

Medical Information Associate/Sr. Associate should review all promotional and educational items according to medical accuracy and compliance.

1. Medical Information Service

Medical Information Associate/Sr. Associate will maintain the highest level of knowledge and up-to date medical/scientific document regarding current disease state and product knowledge (including competitor products), appropriate aspect of regulation and policies

Medical Information Associate/Sr. Associate will disseminate medical information upon customer's unsolicited requests that are:

• scientifically balanced,
• regarding an unsolicited question, and
• meets local requirements.

Medical Information Associate/Sr. Associate will ensure all appropriate sources to answer the inquiries. The followings can be taken of the first priority.

• GML (Global Medical Letter)
• Published articles in scientific journal based on Evidence based medicine (e.g., PubMed, OVID etc.)
• Global Inquiries Database (e.g., Veeva Vault MedComms and Docuvera)
• Global Medical Communication-Information via GCC

All inquiries requested to Medical Information Associate/Sr. Associate must be put in to the service request on GCC(Global Contact Center) and their status, answer and responsibility can be tracked in If a request contains an adverse event, Medical Information Associate/Sr. Associate must report it to Pharmacovigilance Associate/Sr. Associate within 24 hours.

2. Promotional and Educational Material Review

Medical Information Associate/Sr. Associate as a part of medical personnel may participate Promotional and Educational material development plan meeting with brand team in the beginning of planning stage.

All Promotional and Educational Materials must be reviewed by Medical Information Associate/Sr.Associate must review promotional and educational items for medical accuracy and compliance, including checking "Data on file" and all other

references via VVPM (Veeva Vault Promotional Material)

All promotional and educational materials must undergo a local periodic review and approval at intervals of no more than two years via VVPM in accordance with local MIS SOP Promotional and Educational material SOP.

3. Knowledge sharing and training

• Share the good information and knowledge coming from external customers and internal employees.
• Train medical representatives on the value and mission of MIS in various meetings.
• Therapeutic/disease training to MRs and Marketing group on a need basis.
• Develop the educational material for patients related to PSP programs (e.g., Slides, Video etc.)

Minimum Qualification Requirements:

• A bachelor's degree in pharmaceutical sciences, nursing, or other related life sciences
• Be fluent in Korean and English
• Be able to use MS Office and Lilly System
• Be able to demonstrate problem solving, communication skills.
• Understanding the medical materials

Other Information/Additional Preferences:

• Strong communication skills, both verbal and written
• Strong knowledge of MI R&R
• Demonstrated ability to manage large global organizations.
• Project management experience.
• Medical expertise
• Strategic thinking ability based on statistical data.
• Diligent adherence to business integrity principles

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and 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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