Associate Vice President - Women’s Health & Early Clinical Development at Eli Lilly and Company

Boston, Massachusetts, United States

Eli Lilly and Company Logo
Not SpecifiedCompensation
Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, HealthcareIndustries

Requirements

  • MD or MD/PhD in gynecology or reproductive endocrinology, specializing in the health of the female reproductive system
  • Experience providing comprehensive care for conditions including menstrual disorders, preeclampsia, infertility, menopause, and osteoporosis
  • Deep understanding of women’s health physiology, pathophysiology, and clinical care
  • Track record of impactful translational and/or clinical research related to women’s health
  • Demonstrated ability to progress new medicines as part of a drug development team
  • Experience as a clinical researcher in academia or expertise in pharmaceutical drug development

Responsibilities

  • Shape Lilly’s strategy in Women’s Health by combining understanding of the therapeutic landscape and competitive environment with evaluation of internal and external opportunities to build a portfolio
  • Develop project concepts, investment strategies, and clinical development plans for efficient assessment of new therapeutic approaches and targets
  • Collaborate with new product planning to develop and maintain Draft Launch Labels and Value Propositions addressing key customer needs
  • Contribute to and lead innovative drug discovery and development projects
  • Serve as medical expert in interactions with external partners and during assessment of business development opportunities
  • Direct research and clinical development programs through Phase 2
  • Liaise with drug discovery scientists, external innovation, late phase development, and commercial colleagues to evaluate and progress new therapeutic opportunities
  • Advance external collaborations and strategic partnerships to drive impactful outcomes for women’s health
  • Collaborate with clinical research staff in design, conduct, and reporting of clinical trials
  • Review and approve risk profiles to ensure appropriate communication to study subjects
  • Assist in planning and participate in study start-up meetings and other activities to provide training and information to investigators and site personnel
  • Participate in investigator identification and selection
  • Ensure operational team documents completion of administrative requirements for study initiation and conduct consistent with Good Clinical Practices and local laws
  • Serve as resource to clinical operations personnel, clinical research monitors, investigators, and ethical review boards to address questions or clarify issues during study conduct
  • Understand and actively address the scientific information needs of all investigators and personnel
  • Monitor patient safety during clinical trials

Skills

Key technologies and capabilities for this role

Women’s HealthClinical DevelopmentTranslational ResearchClinical ResearchDrug DevelopmentPhase 2GynecologyReproductive EndocrinologyStrategic PartnershipsPortfolio Management

Questions & Answers

Common questions about this position

What qualifications are required for the Associate Vice President role?

The position requires an MD or MD/PhD in gynecology or reproductive endocrinology, with specialization in the health of the female reproductive system, and experience treating conditions like menstrual disorders, preeclampsia, infertility, menopause, and osteoporosis. Clinical researcher experience in academia or expertise in pharmaceutical drug development is also essential.

What are the main responsibilities of this position?

The role involves shaping Lilly’s Women’s Health strategy, developing clinical development plans, collaborating with teams on drug discovery and partnerships, and serving as a medical expert in external interactions.

What is the location or work arrangement for this job?

This information is not specified in the job description.

What is the salary or compensation for this position?

This information is not specified in the job description.

What makes a strong candidate for this AVP role?

A strong candidate is a dynamic strategic leader with deep expertise in women’s health physiology, pathophysiology, and clinical care, a proven track record in translational or clinical research, and experience progressing medicines in drug development teams.

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters
1876Year Founded
$1,180.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.
Potential construction delays in Indiana could affect GLP-1 drug production timelines.
Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.
Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.
FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.
Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.
Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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