Senior Advisor, Clinical Research

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. Job Summary As a Clinical Research Physician at Lilly Suzhou Pharmaceutical Co., Ltd., you will play a pivotal role in the design, execution, and interpretation of clinical trials, contributing to the development of innovative new medicines. Job Responsibilities * Lead or co-lead clinical study design, protocol development, and medical monitoring for assigned clinical trials in accordance with ICH-GCP guidelines and regulatory requirements. * Provide medical expertise and oversight for clinical trial activities, including patient eligibility, safety monitoring, and adverse event reporting. * Collaborate with cross-functional teams, including biostatistics, regulatory affairs, clinical operations, and drug discovery, to ensure seamless execution of clinical programs. * Interpret clinical trial data, contribute to the preparation of study reports, publications, and regulatory submissions. * Participate in investigator meetings, site visits, and scientific conferences to represent Lilly and foster strong relationships with key opinion leaders. * Stay abreast of scientific and clinical advancements in relevant therapeutic areas and apply this knowledge to clinical development strategies. * Ensure compliance with all applicable internal policies, procedures, and external regulations. Job Qualifications * Medical Doctor (MD) degree or equivalent with a valid medical license. * Board certification or significant clinical experience in a relevant therapeutic area (e.g., gene therapy in sensory disease) preferred. * Minimum of 3-5 years of experience in clinical research, either within the pharmaceutical industry, CRO, or academic setting. * Strong understanding of drug development processes, ICH-GCP guidelines, and regulatory requirements (e.g., NMPA, FDA, EMA). * Demonstrated ability to critically evaluate scientific literature and clinical data. * Excellent communication, presentation, and interpersonal skills, with the ability to effectively collaborate with diverse teams. * Fluency in English (written and spoken) is required; proficiency in Mandarin Chinese is highly desirable. 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. #WeAreLilly At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly