Sr. 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 DESCRIPTION

JOB TITLE:

Clinical Research Scientist (CRS) *

BUSINESS UNIT OR AREA:

Exploratory Medicine & Pharmacology (EMP)

LOCATION:

Shanghai

REPORTS TO:

Director-Medical**

SALARY CLASS PROGRESSION:

R3 through R8

SUPERCEDES:

EMP-CRS-CN-v1

PURPOSE OF THE JOB

The Exploratory Medicine & Pharmacology (EMP) Clinical Research Scientist (CRS) participates in the following: responsible to develop, oversee and lead the overall China PK/PD strategy, as well as near- and long-term strategic and scientific focus and vision for China PK/PD strategy. As Subject Matter Expert (SME) for China regulatory guidelines and environment, provide consultation and guidance for other EMP scientists, expert reviewers, and group leaders (as needed) to support PK/PD need in China in China portfolio in all therapeutic areas; responsible for relationship-building with CDE reviewers and local academic/industrial leaders.

JOB REQUIREMENTS

Minimum 5 years’ experiences of experience in PK/PD and Pharmacometrics

Knowledge of drug development process

Fluent in English; both written and verbal communications

Interpersonal, organizational and negotiation skills

Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.

Excellent teamwork skills

Willing to engage in domestic and international travel to the degree appropriate to support the business of the team.

OTHER INFORMATION-role will require interaction with many of the following:

Internal 

Global PK/PD, Modeling & Simulation, ADME, Toxicology

Regulatory directors, scientists, and associates

Therapeutic area Scientists, brand scientists, early phase scientists, and directors-medical

Patient safety scientist

Statisticians

Portfolio & Project Management

Clinical research staff (trial management, site management, data management)

Legal counsel

External

Scientific and clinical experts, thought leaders

Lilly clinical investigators

Practicing Scientists/prescribers

Regulatory agency personnel

Professional association staff and leaders

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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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