Senior Advisor, Clinical Research

Eli Lilly Eli Lilly · Pharma · Shang Hai-上海, China

Senior Advisor, Clinical Research role at Eli Lilly in Shanghai, focusing on the design, execution, and interpretation of clinical trials for new medicines. Requires an MD degree, clinical research experience, and strong understanding of drug development processes and regulatory requirements.

What you'd actually do

  1. 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.
  2. Provide medical expertise and oversight for clinical trial activities, including patient eligibility, safety monitoring, and adverse event reporting.
  3. Collaborate with cross-functional teams, including biostatistics, regulatory affairs, clinical operations, and drug discovery, to ensure seamless execution of clinical programs.
  4. Interpret clinical trial data, contribute to the preparation of study reports, publications, and regulatory submissions.
  5. Participate in investigator meetings, site visits, and scientific conferences to represent Lilly and foster strong relationships with key opinion leaders.

Skills

Required

  • Medical Doctor (MD) degree or equivalent with a valid medical license
  • Minimum of 3-5 years of experience in clinical research
  • Strong understanding of drug development processes, ICH-GCP guidelines, and regulatory requirements
  • Demonstrated ability to critically evaluate scientific literature and clinical data
  • Excellent communication, presentation, and interpersonal skills
  • Fluency in English (written and spoken)

Nice to have

  • Board certification or significant clinical experience in a relevant therapeutic area
  • Proficiency in Mandarin Chinese

What the JD emphasized

  • ICH-GCP guidelines
  • regulatory requirements