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Infectious Disease Clinical Research Physician

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Eli Lilly and Company
Full Time position
Listed on 2026-09-30
Job specializations:
  • Doctor/Physician
    Medical Doctor, Healthcare Consultant, Infectious Disease/ Epidemiology, Internal Medicine Physician
Salary/Wage Range or Industry Benchmark: 243000 - 389000 USD Yearly USD 243000.00 389000.00 YEAR
Job Description & How to Apply Below

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  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…

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