Senior Advisor, Clinical Research, DIA at Lilly

Shanghai, Shanghai, China -

Full Time

Start Date

Immediate

Expiry Date

02 Jul, 26

Salary

0.0

Posted On

03 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research, Medical expertise, Drug development, Endocrinology, Strategic medical planning, Regulatory affairs, Scientific data dissemination, Clinical trial design, Data analysis, Stakeholder management, Cross-functional collaboration, Medical writing, Project management, Budget administration, Scientific training

Industry

Pharmaceutical Manufacturing

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. The primary responsibility of the CRP is to provide expert medical expertise to all aspects of the local business, to ultimately enhance the customers' experience in scientific interaction with Eli Lilly. The CRP responsibility includes development the strategic medical plan for the compound, provide medical expertise for regulatory affairs, providing medical guidance on the business plan, and leading in local scientific data dissemination (leading and presenting at conferences, advisory boards, etc.) The CRP is responsible for collaborating with the global teams in the planning, startup and conduct of phase 3/4 studies (and phase I studies where applicable), as well as non-clinical trial solutions/activities that are conducted in China. In addition, the CRP, if assigned, is responsible for global Development studies conducted in China. The core job responsibilities may include those listed below.Business governance/ Clinical planning (pre and post launch) Ensure life cycle plans for drugs in development address customer needs. Take a leadership role in defining the Patient Journey and corresponding Medical Plan. Become patient advocate, as well as a medical expert. Develop medical strategies to support brand commercialization activities during the development of the local business plan. By offering scientific and creative Input, contribute to the development, review, and approval of promotional materials for the brand team. Provide scientific training of sales representatives, and other function. Scientific Data Dissemination/Exchange Understand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines above. Plan and set up medical symposia, advisory board meetings, and/or the facilitation of other meetings with health care professionals. Prepare or review scientific information in response to customer questions or media requests. Participate in data analysis and the development of publications (abstracts, posters, manuscripts). Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community Clinical Research Take core role and collaborate with clinical research staff in the design, conduct and reporting of local clinical trials. Collaborate with statisticians, health outcomes, research scientists and selected investigators in the development of protocols and data collection requirements. Participate in investigator identification and selection, in conjunction with clinical teams. General Responsibilities Support the business unit management team, including medical leadership in preparation and administration of the local or business unit medical budget. Collaborate proactively and productively with all alliance, business, and vendor partners. Model the leadership behaviors. Be an ambassador of both patients and the Lilly Brand. Job Requirements Medical Doctor of Endocrinology. Must be board eligible or certified in appropriate specialty. 3-5 years of Clinical practice or clinical research experience. Pharmaceutical medical function experience is preferred. Knowledge of drug development process is preferred Demonstrated ability to balance scientific priorities with business priorities Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment. Ability to engage in domestic and international travel to the degree appropriate to support the business of the team. Fluent in English, verbal and written communication. 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

Responsibilities

The Senior Advisor provides medical expertise to support the local business, including developing strategic medical plans and leading scientific data dissemination. They also collaborate with global teams to manage clinical trials and ensure life cycle plans address patient needs.