Lilly Jobs

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.

Overview:

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Purpose:

The Sr. Director-Medical is delegated various responsibilities by the Associate Vice-president or equivalent role to provide leadership, supervision, coordination, coaching, career development, and performance management for the staff within a specified therapeutic or product subgroup of Development in the Business Unit. The position is a developmental role for future administrative leaders and is intended to provide a balance of administrative and technical responsibilities. The position requires a partial transition from direct CRP contributor to managerial/supervisory responsibilities and activities of achieving results through others, and supporting the management team in fulfilling corporate goals and initiatives. The Sr. Director-Medical will provide strong leadership, ability to influence, both within and outside the team. The Sr. Director-Medical

supports the clinical staff within his/her product or therapeutic group to ensure high quality, timely submissions, and successful commercialization. The Sr. Director-Medical may be delegated such responsibilities as approval authority for grants and contracts, protocols and protocol amendments, label changes, scientific e-disclosure, informed consent documents, travel authorizations, expense reports, and other documents related to the work of the group.

In addition to his/her focused administrative responsibilities, the Sr. Director Medical participates in strategic planning for and oversight of the clinical research and medical support activities of the Director's area of responsibility. The Sr. Director-Medical will also interact with external consultants, opinion leaders, and worldwide regulatory agencies, and will provide oversight for responding to medical and regulatory questions and requests related to products. The Sr. Director-Medical helps to ensure that the team's activities are clearly aligned with Global Patient Safety (GPS), and as appropriate, with Program Phase Medical and Clinical Pharmacology. The Sr. Director-Medical plays a significant role in submission, registration, and product launch. In this role, the Sr. Director-Medical maintains close contact with relevant local and global clinical research management, marketing management, and corporate teams. In the absence of the Associate Vice-president -Medical, the Sr. Director-Medical may carry out certain responsibilities of the AVP. The Sr. Director-Medical maintains the ongoing responsibilities of a Clinical Research Physician for product support and clinical research in his/her area (see area job description for CRP for review of core job responsibilities), adjusted and balanced to the level and extent as appropriate to correspond to the needs of the area and role.

The Sr. Director-Medical is aware of and ensures that all activities of the medical team are in compliance with current local and international regulations, laws, guidances (e.g. FDA, ICH, CPMP etc.), Good Clinical Practices (GCPs), company

standards, Lilly policies and procedures, company integrity agreements as applicable, and the Principles of Medical Research and are aligned with the medical vision.

Primary Responsibilities:

1. Career Development and Performance Management of direct reports

• Works closely with direct reports, to develop their performance management plans (objectives), development plans, corporate resumes, performance appraisals.

• Keeps all performance and career related documents and plans for direct reports up to date.

• Meets regularly with each direct report to coach, mentor, evaluate progress toward objective fulfillment, evaluate training and development needs, and monitor career development goals.

• Maximizes each individual direct report's career potential, maximizing the value to the corporation.

• Responsible for retaining talented people for the long term.

• Responsible for presenting the activities, desires, capabilities, and achievements of direct reports to the Associate Vice President, Medical management group, HR, and Global Medical Capabilities and Development department for talent assessment, performance evaluation, and timely promotion consideration.

• Accountable for CRP/S capacity planning and work allocation.

• Recognizes and appropriately rewards exceptional performance, talent, and/or contribution.

• Lead and appropriately delegate to the physicians and clinical research scientists on the team who are responsible for clinical development plans.

• Ensures that all direct reports are adequately qualified and trained in the tasks they are required to perform. Includes accountability and compliance for maintaining a current curriculum training map for self and direct reports.

2. Oversight of clinical planning, budgeting and execution

• Respect the value and contributions of paramedical technical talent on the team.

• Partner with cross-functional team members to assist the Associate Vice president in the development of the clinical strategy and clinical plans.

• Partner with the medical leadership in effective budget planning and integration of clinical/business plans.

• Ensures placement of the clinical welfare of patients and subjects using a Lilly product or participating in a Lilly clinical investigation above all other considerations.

• Ensures medical group meets or exceeds commitments for planned and agreed upon clinical research.

• Monitors progress toward implementation of the clinical research plans, and takes appropriate steps with the responsible clinical plans personnel and CRPs if progress is not adequate.

• Monitors progress toward implementation of the other deliverables from the medical team and take appropriate steps with the responsible cross-functional management team(s) if progress is not adequate.

• Works closely with the Associate Vice President to monitor operational expenses of the group, and takes appropriate actions if there are substantial deviations from approved budgets.

3. Scientific and Technical Expertise

• Maintains his/her deep scientific, technical expertise and support, conducting activities in clinical research, submission, and commercialization support balanced with administrative activities as agreed upon by Sr. Director-Medical.

• Provide technical expertise, protocol development oversight, and input into development of informed consent documents.

• Understand and keep updated with the pre-clinical, clinical pharmacology, and clinical data relevant to the team molecule.

• Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the team.

• Role model and functional member of the appropriate research, submission, registration, and commercialization support teams.

• Visibly active in business unit/ therapeutic area to maintain credibility with internal and external colleagues and the larger organization, as well as to enhance career satisfaction.

4. Scientific Data Dissemination and Exchange

• Ensures timely dissemination of clinical trial data.

• Help to ensure the critical analysis of data and the dissemination of that data, including but not limited to manuscripts, abstracts, posters, and slide sets. Works closely with statistical and global scientific communications colleagues.

• Support the planning of symposia, advisory board meetings, and other meetings with health care professionals.

• Oversight of team's attendance and scientific 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)

5. Regulatory/Submission Responsibilities

• Ensures that clinical data generated for regulatory purposes meets all necessary regulatory standards.

• Provide support for global registrations, labeling and label modifications, and resolution of regulatory issues.

• Advisory committee participation as assigned.

6. Overall Administrative Responsibilities

• Serves as a member of the business unit development management team, and as such attends meetings, and contributes to area management process and policy development as requested by Associate Vice President.

• Participates in various projects, committees, task forces, and other discrete efforts as requested by executive management.

• Participates in activities which includes, but not limited to overall area plans and budgets, strategic planning, support of efforts of other components such as staff recruiting, and participation on various corporate or cross-functional

committees.

• Ensures that new process improvement initiatives and best practices are implemented.

• Ensures that team members respect the highest medical ethical standards of Lilly and of the communities where Lilly does business.

• May participate in succession planning for the area.

• May participate in annual business planning for local activities with the Associate Vice President

• Approval responsibility for the entire group remains with the Associate Vice President. The Sr. Director- Medical may be delegated responsibilities or serve as the backup for the Associate Vice President for review of major business documents requiring director-level approval in his/her absence. These documents include, but are not limited to research protocols and amendments, research contracts and grants, informed consent documents, label changes, and travel expenses.

• Reviews and approves other types of documents in the absence of Associate Vice President or CRP/S

• Responsible for disseminating information and communications to his/her direct reports and colleagues.

• Ensure collaboration between team members and Global Patient Safety (GPS).

• Coordinate collaborations with other business unit CRPs, Program Phase and Clinical Pharmacology, and Discovery colleagues as necessary.

• Serves as liaison with affiliates/geographical regions as assigned by Associate Vice President

• Provide coaching and feedback to other team members.

7. Additional Corporate Responsibilities

• As a member of the management team, is an active and visible representative of the corporate function.

• Be an effective partner/team player with other functions.

• Serves as a role model for and representative of physicians for the team in other organizational venues (e.g., corporate review committees).

• Serves as a representative of the global brand team to groups, committees, or agencies outside the company or the industry as assigned by Sr. Director-Medical.

9. Recruitment

• Participates with the Associate Vice President, in conjunction with the business unit and DCOE for determining the human resource needs for the development area and overseeing implementation of the staff recruiting plan, supported by executive management, Human Resources and Global Medical Capabilities and Development.

• Successful recruiting of clinical research physicians (CRPs) or clinical research scientists (CRSs) for the area requiring involvement and a potential for substantial time commitment.

Minimum Qualification Requirements:

▪ Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring. US trained physicians must have achieved board eligibility or certification.

▪ Medical specialty in at least one of the following: Allergy, Immunology, Pulmonology.

▪ Minimum two years experience in clinical research/drug development including the design and implementation of large global clinical trials

Additional Preferences:

▪Demonstrated Medical Advisor technical status (or equivalent)

▪ Demonstrated evidence for the capacity to lead and manage groups of professionals

▪ Demonstrated administrative skills, including strong team work skills

▪ Demonstrated evidence of the ability to work within Lilly's governance structure

▪ Demonstrated experience with strong communication, interpersonal, and negotiation skills

▪ Ability to travel away from office, both domestic and international to the degree appropriate to support the business of the team.

▪ Fluent in English, verbal and written communication

▪ 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

Physicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer.

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 ( LillyRecruitingCompliance@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 is an EEO/Affirmative Action Employer and 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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

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