Purpose:
- The purpose of this role is to provide leadership for Case Management Medical Review Therapeutic Area hubs. In particular,
- leadership will be provided through direct technical and administrative leadership of a global team of therapeutically aligned
- Case Management Medical Review physicians and scientists. They will work in close collaboration with and report to the Senior
- Director/Executive Director u2013 Case Management Medical Review and will collaborate with leaders globally responsible for
- Medical Review and Case Management.
Primary 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 supervisor regarding your actual job responsibilities and any related duties that may be required for the position.
1. Leadership in Medical Review:
- u00A0Supervise Case Management Medical Review personnel within the therapeutic area across the global team including physicians and scientists.
- u00A0Build deep regulatory and technical expertise through recruitment, development, and retention of staff.
- u00A0Facilitate, train and mentor Case Management Medical Reviewers in the responsibilities of the role.
- u00A0Provide feedback and coaching, support short and long-term development plans, and ensure appropriate individual recognition.
- u00A0Oversee the medical evaluation of safety of Individual Case Safety Reports for all assigned compounds across their life cycle to inform the safety profile of the therapeutic area portfolio.
- u00A0Develop, maintain, and share technical expertise and medical knowledge in the therapeutic area.
- u00A0Provide strong global medical leadership that influences scientific and process improvements and drive change within the organization.
- u00A0Lead and participate in process improvement and innovation projects to support the safety of all assigned compounds.
- u00A0Participate in the development and implementation of the functional strategic plan for Case Management Medical Review.
- u00A0Manage resources to meet business objectives and future needs within the therapeutic area in collaboration with leaders across the global team.
- u00A0Collaborate cross-functionally to ensure alignment of goals and deliverables, readjusting as business needs dictate.
- u00A0Partner closely with global GPS partners for efficient resource forecasting, planning, and utilization to meet business objectives.
2. Enterprise Leadership:
- Lead actions and collaborate with GPS teams to ensure appropriate interaction, communication, and high-quality medical evaluation of safety within the therapeutic area.
- Act as a Lilly Case Management Medical Review representative for both internal and external customers, interacting as described in corporate guidelines and policies.
- u00A0Build strong relationships with key customers, representing and championing the role of safety in the organization.
- u00A0Collaborate with Affiliates, Business Units, and Clinical Development teams re garding areas of relevant medical review expertise and responsibility.
- Lead actions required to manage or clarify a safety issue in collaboration with the responsible global teams.
3. Understand the roles and responsibilities of the EU qualified person (QP) and ensure support to the fulfillment of QPu2019s legal responsibilities is provided when required.
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. Foreign medical graduates (in US based jobs) 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.
- Non-US trained physicians must have completed education and training at a medical school that meets the minimum requirements substantially equivalent to the requirements of medical schools accredited by the Liaison Committee on
- Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see PLA: Physicians Licensing Information and Medical Education | MBC.
- Clinical development or pharmacovigilance experience preferred.
- Knowledge of drug development process.
- Fluent in English with highly effective written and verbal communication skills.
- Strong clinical/diagnostic skills.
- Excellent interpersonal, organizational and negotiation skills.
- Ability to work on multiple projects and function effectively in a fast-paced matrixed environment.
- Ability to prioritize tasks and shift priorities rapidly to meet tight deadlines
- 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/Additional Preferences:
- 3+ years of prior people management experience.
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 () 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.
Lillyu00A0does 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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