Eli Lilly and Company

The Principal Scientist Sample Management will work closely with leadership and team members to help operationalize and maintain a compound management operation.. Experience with inventory/request database systems for compound and/or biological sample management (LIMS).. Excellent written, verbal, and interpersonal communication skills are required, with ability to work with/across a range of disciplines including biology, medicinal chemistry and bioassay.. Collaborate with other functional areas (Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics organization) in the development of methods for assessing special clinical safety pharmacology studies.. 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.

principal scientist

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. About Loxo Oncology At Lilly Loxo@Lilly conducts discovery research, clinical development, and regulatory affairs for oncology, with the goal of creating a pipeline of therapies that have the potential to make a meaningful difference for patients. Loxo Oncology at Lilly was created in December 2019, combining the Lilly Research Laboratories oncology organization and Loxo Oncology, which was acquired by Lilly in early 2019. The unit has team members in Boulder, CO, Indianapolis, IN, New York City, NY, South San Francisco, CA, San Diego, CA, Stamford, CT, and Madrid, Spain. Position Summary The Principal Scientist Sample Management will work closely with leadership and team members to help operationalize and maintain a compound management operation. This team will be accountable for establishing and executing SOPs and processes related to storage of inventory, preparation of samples for testing, and shipping/receipt of supplies/samples/compounds for internal/external assays. This role will support compound management activities across multiple geographies, multiple departments and external CROs. Roles And Responsibilities <ul><li>Assist in implementation of recently purchased capital equipment for expansion of the compound management operation and implement plans for long term, sustainable instrument maintenance.</li><li>Maintain and improve sample workflows associated with storage, manual neat/weigh operations, liquid handling, and delivery of samples to internal and external teams.</li><li>Provide compound registration support.</li><li>Develop tools to simplify internal processes and improve user experience.</li><li>Manage processes associated with international and domestic shipments between collaborators and research sites, ensuring proper documentation is maintained.</li><li>Establish/Maintain a generative safety culture and ensure adherence to safety policies.</li><li>Serve as a steward for the physical compound inventory as well as the associated inventory/output data.</li><li>Test/Validate changes to software, hardware, and procedures. Proactively seek improvements to usability of these systems and production timelines.</li><li>Create and maintain SOPs and job aids for critical processes.</li><li>Troubleshoot software and hardware issues and resolve sample dispensing issues raised by customers.</li><li>Assist laboratory technicians with day-to-day responsibilities, ensuring projects are supported in a timely, consistent manner.</li><li>Establish processes for replenishment of consumables.</li><li>Track production metrics to quantify required changes and subtle operational issues.</li><li>Assist in development, deployment, and change management of enterprise level sample management software</li><li>Continue customization of sample software, and work closely with vendors to solve problems</li><li>Maintain effective oral and written communication to Discovery team members (and beyond) and provide support to ensure timelines are met.</li><li>Maintain customer-focused attitude and operation.</li><li>Provide additional support to the Discovery Team (and beyond) as needed. </li></ul>Required Qualifications <ul><li>A BS/MS or equivalent degree in chemical, biological, engineering sciences or related field with 5+ years working full time in a laboratory setting either in academia or industry.</li><li>Experience programming and maintaining laboratory instruments/automation related to compound management (e.g., storage systems, balances, traditional and acoustic liquid handlers)</li><li>Experience maintaining an inventory of neat and solubilized samples.</li><li>Experience with inventory/request database systems for compound and/or biological sample management (LIMS).</li><li>Strong organizational skills and attention to detail.</li><li>Ability to work both independently and within a multidisciplinary team.</li><li>Excellent written, verbal, and interpersonal communication skills are required, with ability to work with/across a range of disciplines including biology, medicinal chemistry and bioassay. </li></ul>Additional Skills <ul><li>Experience with software and hardware components of relevant automation platforms such as Beckman Echo, Tecan, High Res Biosystems, and automated storage (Hamilton and/or Azenta)</li><li>Experience with automation controlling software such as Cellario, Green Button Go or similar.</li><li>Experience scripting in any relevant languages</li><li>Experience shipping/receiving both domestically and internationally. </li></ul>Loxo@Lilly (Eli Lilly and Company) currently anticipates that the base salary for this position could range from between $69,000-195,800 and will depend, in part, on the successful candidate’s qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Loxo@Lilly (Eli Lilly and Company) offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibilit 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. Eli Lilly Cork is made up of a talented diverse team of over 1,600 employees across 38 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more. Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’ wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues. Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, Age & Culture, LGBTQ+ and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all. Together they are committed to promoting awareness to create a disability confident culture both at Eli Lilly Cork and beyond. Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself. Responsibilities Through the application of pharmacological training, expertise and relevant therapeutic area experience , the Clinical Pharmacologist (CP) participates in the following: 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; and the outreach activities aimed at the external clinical customer community, including thought leaders. In addition, the CP works with the basic research scientists to identify lead compounds and plan pre-clinical studies as well as network with the Business Unit to plan for the clinical pharmacology submission package. The CP serves as a scientific resource for study teams, departments, and others as needed. The CP is aware of and ensures that all activities of the medical team are in compliance with current local and international regulations, laws, guidance (e.g. FDA, ICH, and CPMP etc.), Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, and the Principles of Medical Research and are aligned with the medical vision. Core Job Responsibilities The primary responsibilities of the CP are generally related to clinical pharmacology including early phase exploratory and late phase biopharm submission studies. The core job responsibilities may include those listed below as deemed appropriate by line management, as well as other duties as assigned. Clinical Planning <ul><li>Contribute to the development of the overall strategy and clinical plan for development of clinical compounds, focusing on studies required for product decision or regulatory submission.</li><li>Support preparation of high-level plan for phase 2 and 3 studies for early phase and/or detailed biopharm plan to support submission.</li><li>Collaborate with other functional areas (Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics organization) in the development of methods for assessing special clinical safety pharmacology studies.</li><li>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.</li><li>Contribute, as an integral member of the Clinical Pharmacology team, to global Phase I and II clinical studies as well as submission planning activities.</li><li>Work closely with discovery research scientists in the development of basic research strategies, clinical candidate compound selection, and pre-clinical development.</li><li>Work with Brand Team/Business Unit colleagues to provide appropriate market differentiation and regulatory support in the biopharm submission plan. </li></ul>Clinical Research/Trial Execution and Support <ul><li>Design and oversee implementation of all clinical pharmacology studies. Capabilities include understanding the unique aspects of conducting such studies in healthy volunteers and patient groups/special populations.</li><li>Apply fundamental concepts of clinical pharmacology and clinical pharmacokinetics to clinical pharmacology research.</li><li>Design and oversee implementation methods for development and biomarker qualification studies.</li><li>Design, create, and provide oversight for protocol development.</li><li>Support development of documents for the conduct of studies in collaboration with functions and operations staff and affiliates in accordance with GCP and local requirements.</li><li>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.</li><li>Participate in investigator identification and selection, in conjunction with the clinical pharmacology sourcing group.</li><li>Review and provide input to risk profiles and local informed consent documents as required, ensuring appropriate communication of risk to study subjects.</li><li>Provide oversight ensuring 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.</li><li>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.</li><li>Serve as resource to clinical trial managers, clinical research monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study.</li><li>Understand and actively address the scientific information needs of all investigators and personnel.</li><li>Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with global patient safety policies and procedures.</li><li>Implement and communicate appropriate pharmacovigilance actions as needed during conduct of the study in collaboration with global patient safety.</li><li>Provide appropriate oversight and partnership with Third Party Organizations to ensure successful study execution. </li></ul>Scientific Data Dissemination/Exchange <ul><li>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.</li><li>Address the unsolicited scientific questions and information needs of external health care professionals according to guidelines above.</li><li>Participate in reporting of clinical trial data in Clinical Trial Registry activities.</li><li>Partner with NPP (New Product Planning) and scientific communications staff on publication strategy and process.</li><li>Prepare and present documentation of clinical trial results to corporate committees, regulatory agencies, and other external agencies.</li><li>Publish results of research projects as appropriate.</li><li>Consider, review or develop pharmacoepidemiologic (quality of life, cost/effectiveness) and health economic aspects.</li><li>Support the planning of symposia, advisory board meetings, and other meetings with health care professionals.</li><li>Participate in data analysis, development of scientific data dissemination, and preparation of final reports and publications for clinical pharmacology-biopharmaceutical trials.</li><li>Provide clinical reports for local and international regulatory purposes. </li></ul>Regulatory Support Activities <ul><li>Support I 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. </li></ul>People Management And Development <ul><li>Develop, and retain a scientifically excellent, innovation-minded, highly capable workforce with strong exploratory medicine experience</li><li>Build an organizational culture that fosters inclusion and innovation, continual improvement, and with an external understanding and awareness</li><li>Develop an organizational talent base that demonstrates judgment-based risk taking and decision making </li></ul>Basic Qualifications <ul><li>Life science degree (MD, PhD, PharmD) with requisite experience in Clinical Pharmacology – A minimum of 10 years work experience in Clinical Pharmacology</li><li>Minimum of 5 years of professional experience in pharmaceutical drug development with demonstrated experience and knowledge of clinical research and the drug development process. </li></ul>Additional Skills/Preferences <ul><li>PhD preferable but not required</li><li>Experience in Pharmaceutics and Product Design preferable</li><li>Knowledge of and experience in Clinical Pharmacology and drug development process preferred</li><li>Fluent in English; both written and verbal communications</li><li>Interpersonal, organizational and negotiation skills</li><li>Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.</li><li>Excellent teamwork skills.</li><li>Willing to engage in domestic and international travel to the degree appropriate to support the business of the team. </li></ul>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 ( Lilly_Recruiting_Compliance@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 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. #WeAreLilly

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