Director - Medical - Clinical Research Physician

Regulatory Toolkit; Indianapolis (IN); Hybride; USD 201 000 - 394 000; Plein temps

Avantages offerts par ce poste

Company bonus

401(k) plan

Medical/dental/vision benefits

Résumé du poste

Lilly in Indianapolis is seeking a Clinical Research Physician for the Cardiometabolic Research (CMR) Program. The role focuses on early-phase compound development, global trial execution, regulatory support, and scientific data dissemination.

Collaboration with local and international investigators, pharmacology and PK/PD teams is essential to optimize study design and patient outcomes. You will oversee Phase I–IIb studies, design protocols, monitor safety, and contribute to strategic trial

Qualifications

• Must be Medical Doctor or Doctor of Osteopathy and board eligible/certified.
• US-trained physicians must have board eligibility or certification.
• Non-US trained physicians must have LCME-equivalent education and training.
• Fluent in English; strong written and verbal communication.
• Willing to travel domestically and internationally as required.

Responsabilités

• Design and oversee Phase I–IIb clinical studies and contribute to phase planning.
• Write and review clinical trial protocols and development plans.
• Collaborate with investigators, consultants and staff globally on protocols and data collection.
• Monitor patient safety and adverse events per corporate safety policies.
• Support regulatory reporting, labeling discussions and dissemination of results.
• Lead and participate in scientific communications, publications and congress activities.

Connaissances

Fluent English

Interpersonal skills

Organizational skills

Negotiation skills

Teamwork

Willing to travel

Formation

MD or DO

Board eligibility/certification

Description du poste

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

The Cardiometabolic Research (CMR) Program Clinical Research Physician (CRP) participates in the following for compounds of responsibility for the therapeutic area, including an evolving portfolio of compounds targeting women’s health: the development, conduct and reporting of global clinical trials for new compounds, the implementation of global clinical trials, the reporting of adverse events as mandated by corporate patient safety; the review process for protocols, study reports, publications and data dissemination for products, new and updated labels, grant submissions and contracts, contacts with regulatory and other governmental agencies; assessment of licensing opportunities, and the outreach activities aimed at the external clinical customer community. In addition, the Clinical Research Physician works with research scientists to identify lead compounds and clinical candidates and plan pre-clinical studies. Core tasks will be delegated based on level of experience.

Other activities include internal training activities, peer-review of clinical protocols and reports, and ad hoc scientific consultation within Lilly. The CRP works with late stage development colleagues to plan for meeting patient needs through clinical studies, and outcomes and pharmacoeconomic research.

Responsibilities:

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

The primary responsibilities of the CMR Program Phase CRP are generally related to early-phase compounds, including those targeting women’s health.

The core job responsibilities may include those listed below as deemed appropriate by line management, as well as other duties as assigned.

Clinical Planning

• Contribute to the development of the overall strategy and clinical plan for development of clinical compounds, focusing on studies required for product decision. Support preparation of high-level plan for phase Ill studies.
• Collaborate with local clinical research staff, consultants and clinical investigators in the design, conduct and reporting of global Phase lb and Ila/IIb clinical trials (e.g., sample size, patient commitment, timelines, grants, and governance review interactions).
• Collaborate with other quantitative scientists (e.g., PK/PD, statistics, molecular epidemiology, ADME, modeling and simulations) to integrate study development and conduct with disease-progression and drug disease response models.
• Work closely with discovery research scientists in the development of basic research strategies, clinical candidate compound selection, and pre-clinical development.
• Collaborate with non-clinical pharmacologists to translate observations from animal experiments to human clinical studies (biomarker development) in the area therapeutic area of responsibility.
• Collaborate with drug disposition scientist to conduct pharmacokinetic and drug metabolism studies of drug candidates in humans.
• Assist pharmacokineticists and statisticians by providing clinical support to the development of pharmacostatistical models of drug exposure and response (PK/PD modeling and trial stimulation) to optimize dosing regimens and selection of the target patient population.

Clinical Research/Trial Execution and Support

• Design and oversee implementation of Phase lb and Ila/IIb clinical studies.
• Design and write clinical trial protocols.
• Design and oversee implementation methods for development and biomarker qualification studies.
• Collaborate with local clinical research staff, statisticians, health outcomes research scientists and selected consultants and/or investigators in the development of protocols, and data collection requirements.
• Participate in investigator identification and selection, in conjunction with clinical team.
• Interact with consultants and clinical investigators to plan, initiate, and conduct worldwide clinical trials (Phase I and II).
• Review and approve risk profiles, and local informed consent documents as required, to ensure appropriate communication of risk to study subjects.
• Ensure that operational team has documented the completion of administrative requirements for study initiation and conduct (i.e., ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local laws and requirements.
• Assist in planning process and participate in study start-up meetings and other activities to provide the appropriate training and information to investigators and site personnel.
• Serve as resource to CDAs I clinical research monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study.
• Understand and actively address the scientific information needs of all investigators and personnel.
• Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures.

Scientific Data Dissemination/Exchange

• Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals/customers.
• Understand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines above.
• Participate in reporting of clinical trial data in Clinical Trial Registry activities.
• Consider, review or develop pharmacoepidemiologic (quality of life, cost/effectiveness) and health economic aspects.
• Support the planning of symposia, advisory board meetings, and other meetings with health care professionals.
• Participate in data analysis, development of scientific data dissemination and preparation of final reports.
• Support development of slide sets and publications (abstracts, posters, manuscripts).
• Support the creation and review of any scientific information with respect to customer questions or media request in accordance with global compliance policies and procedures.
• Provide congress support (e.g., availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events).

Regulatory Support Activities

• Support/ assist in the preparation of regulatory reports, including the medical sections of the IND and Investigator Brochure, preparation of FDA advisory committee regulatory hearings and label discussions, and communications and resolution of regulatory issues, including regulatory response.
• Develop and review labeling modifications in collaboration with regulatory and safety groups.
• Participate in risk management planning along with GPS colleagues.
• Provide medical expertise to regulatory scientists.

Business/ customer support

• Understand the scientific/medical needs of all CMR Program Phase customers (payers, patients, health care providers
• Provide advice and consultation to global business unit with regard to potential markets for development compounds and in-licensed projects or compounds.
• Support business development in collaboration with the regulatory and corporate affairs group.
• Establish and maintain appropriate collaborations and relationships with external experts, thought leaders, and the general medical community on a national and possibly international basis.
• Participate in PhRMA or other local or national trade associations.
• Develop and maintain appropriate collaborations and relationships with relevant professional societies.
• Participate in patent development.
• Take a leadership role in defining the Patient Journey and corresponding Moments of Truth based on his/her medical knowledge. Become a patient advocate, as well as a medical expert.

Scientific & Technical Expertise and Continued Development

• Critically read and evaluate the relevant medical literature; know the status and data in medical field of interest; and keep updated with medical and other scientific developments relevant to the therapeutic area.
• Provide consultation to health outcomes staff, marketing professionals, and management regarding the potential medical need served by responsible therapeutic area drug candidates.
• Knowledge of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the development projects.
• Explore and take advantage of opportunities for extramural scientific experiences.
• Attend scientific symposia.
• Understand and keep updated with the pre-clinical, clinical pharmacology and clinical data relevant to the molecule.
• Maintain awareness of current clinical practices through experience or contacts.

General Responsibilities

• Actively set and meet individual professional development goals and contribute to the development of others by being an active source of coaching and feedback to co-workers.
• Actively participate in recruitment, diversity, and retention efforts.
• Participate in committees, initiatives and task forces as requested by local/corporate management.
• Model leadership behaviors and lead matrixed cross-functional teams.
• Be an ambassador of both patients and for the Lilly Brand.

Basic Qualifications/Requirements:

• Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in a medical specialty or have completed the comparable level of post‑medical school clinical training relevant to the country of hiring. U.S. trained physicians must have achieved board eligibility or certification. Foreign medical graduates in U.S. based jobs, who are not U.S. board eligible or certified may be hired directly for employment in the U.S. at the discretion of the Chief Medical Officer.
• Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see http://www.in.gov/pla/2799.htm

Additional Information :

• Board certified or eligible in Obstetrics and Gynecology, Endocrinology, Immunology preferred.
• Clinical research or pharmaceutical medicine experience preferred.
• Knowledgeofdrug developmentprocess preferred.
• 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.

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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$201,000 - $393,800

Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well‑being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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