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Infectious Disease Clinical Research Physician

Key Facts

Remote From: 
Full time
Senior (5-10 years)
Japanese

Other Skills

  • Team Leadership
  • Communication
  • Analytical Skills
  • Ethical Standards And Conduct
  • Teamwork
  • Critical Thinking
  • Social Skills
  • Problem Solving

Roles & Responsibilities

  • Medical Doctor (M.D.) or Doctor of Osteopathy (D.O.)
  • For non-U.S. trained physicians, education and training must be at LCME-accredited medical school
  • Board eligible or certified in the appropriate specialty/subspecialty, or comparable post-medical school training; U.S.-trained physicians must have board eligibility or certification
  • Minimum of 5 years of experience in clinical research within the pharmaceutical industry or academic research setting

Requirements:

  • Design and develop clinical trial protocols, statistical analysis plans, and other essential study documents for infectious disease programs
  • Serve as a medical expert for assigned clinical trials, providing medical input and oversight throughout the study lifecycle, including site selection, investigator meetings, and data review
  • Monitor and interpret clinical trial data, identifying safety signals, efficacy trends, and potential issues, and proposing appropriate actions
  • Lead and participate in interactions with regulatory authorities (e.g., FDA, EMA) regarding clinical trial design, data submission, and labeling

Job description

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.

Eli Lilly and Company is seeking an experienced and passionate Infectious Disease Clinical Research Physician to contribute to the development of novel therapies. This role involves designing, executing, and interpreting clinical trials for infectious diseases, ensuring scientific rigor and ethical conduct.

Responsibilities:

* Design and develop clinical trial protocols, statistical analysis plans, and other essential study documents for infectious disease programs.
* Serve as a medical expert for assigned clinical trials, providing medical input and oversight throughout the study lifecycle, including site selection, investigator meetings, and data review.
* Monitor and interpret clinical trial data, identifying safety signals, efficacy trends, and potential issues, and proposing appropriate actions.
* Lead and participate in interactions with regulatory authorities (e.g., FDA, EMA) regarding clinical trial design, data submission, and labeling.
* Collaborate effectively with cross-functional teams, including preclinical research, biostatistics, regulatory affairs, clinical operations, and commercial teams, supervising teams as assigned.
* Contribute to the preparation of clinical study reports, publications, and presentations at scientific conferences.
* Provide medical expertise and guidance to internal project teams and external investigators.
* Stay abreast of scientific and clinical developments in infectious diseases and clinical research methodology.
* Ensure compliance with all applicable regulations, Good Clinical Practice (GCP), and company standard operating procedures (SOPs).

Basic Qualifications:

* Medical Doctor (M.D.) or Doctor of Osteopathy (D.O.). Non-U.S. trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see PLA: Medical Licensing Information  and Medical Education | MBC.

* Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. 

* U.S. trained physicians must have achieved board eligibility or certification. Foreign medical graduates in U.S. based jobs, who are not U.S. board eligible or certified may be hired directly for employment in the U.S. at the discretion of the Chief Medical Officer.

* Minimum of 5 years of experience in clinical research within the pharmaceutical industry or academic research setting.

Additional Preferences:

* Board eligibility or certification in pediatric or adult infectious disease is highly desirable.

* Pharmaceutical industry or academic research with a significant focus on infectious diseases.

*Demonstrated experience in designing, conducting, and interpreting Phase 1, 2, or 3 clinical trials.
* Strong understanding of drug development processes, regulatory requirements, and GCP guidelines.
* Excellent communication, interpersonal, and presentation skills.
* Ability to work independently and collaboratively in a fast-paced, matrixed environment.
* Proven ability to critically analyze and interpret complex scientific and clinical data.

* Experience with global clinical trials is highly desirable.
* Publications in peer-reviewed medical journals are a plus.

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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$243,000 - $389,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

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