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. **Position Summary:** The Senior Director, Clinical Development will lead clinical development program(s) in support of overall clinical development strategy and vision and serve as liaison and resource to various physicians and clinical trial sites, drawing on strong medical and scientific knowledge/principles, understanding of compliance and regulatory requirements as well as awareness across business operations, and emerging issues. **Responsibilities:** Primary responsibility for and ownership of design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. + May participate in or lead clinical development contributions for due diligence or other business development activity. As required by program needs, contributes in partnership with research colleagues to design and implement translational strategies. + Acts as clinical lead and actively solicits opinion leader interactions related to the disease area(s); partners with cross functional teams as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate. + Stays abreast of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area. May represent Lilly at key external meetings. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. **Minimum Requirements:** + Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in Oncology or Hematology (or equivalent) or have completed the comparable level of post-medical school clinical training relevant to the country of hiring + 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 (https://www.in.gov/pla/professions/physicians-home/physicians-licensing-information/#Approved\_Disapproved\_Foreign\_Medical\_Schools) + 5+ years Clinical Trials/Research experience in pharmaceutical industry, academia, research setting or equivalent. **Additional Preferences:** + PhD would be highly advantageous. + Proven leadership skills and ability to bring out the best in others on a cross-functional global team. Must be able to lead through influence. + Proven ability to interact externally and internally to support a global scientific and business strategy. + Strong document management skills, including proficiency with MS Word, EndNote, PowerPoint, and Excel. + Demonstrated ability to work well with other accomplished professionals within and across functions/teams. Willing collaborator. + Strong communication skills both written and oral. + Ability to multi-task and shift priorities rapidly to meet tight deadlines. + Ability to exercise judgment and address complex problems and create solutions for one or more projects. + Ability to develop collaborative working relationships with physicians, expert consultants, and contracted vendors. + Strong analytical mind and problem-solving skills, attention to detail, strong organizational skills, and ability to work independently and as part of a team. **Additional Information:** **Physical Demands/Travel:** + The physical demands of this job are consistent with an office/remote office environment **. This role will require global travel.** + _The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job._ **Work Environment:** + This position’s work environment is in an office/remote office. + _The_ _work_ _environment_ _characteristics_ _described_ _here_ _are_ _representative of those an employee encounters while performing the essential functions of this job._ 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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $198,000 - $336,600 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. \#WeAreLilly