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Lilly Consultant - Clinical Development / Northeast United States (territory includes New York, Connecticut, Rhode Island, Maine, Massachusetts, New Hampshire, Vermont) in Jefferson City, Missouri

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 39,000 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.

Organization Overview:

At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world’s greatest health challenges.

The Clinical Development Consultant (CDC) is responsible for the management of clinical sites being considered and/or participating in Lilly clinical trials; inclusive of site identification and qualification, the on time delivery of clinical trial enrollment in accordance with scientific objectives, prompt delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic area(s) within a region/country that enables global program delivery. This is achieved by the CDC’s accountability for comprehensive site management, optimize the use of information to make informed decisions. Engage in high quality interactions with global clinical trial sites to drive to an unparalleled customer experience. The CDC is also responsible for oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends. Additional local responsibilities may be required as needed/appropriate for the local geography.

Primary Responsibilities:

Clinical Investigator Management

Accountable for the following:

  • Activities required at clinical trial sites and by investigators and site staff participating in Lilly trials; inclusive of site identification and qualification, enrollment planning and execution, to database lock and close out

  • Comprehensive site management activities to ensure prompt delivery of enrollment readiness, trial recruitment/enrollment and database locks; inclusive of performance management and issue mitigation, identification and resolution

  • Identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience

  • Application of scientific, therapeutic area, and institutional/regional expertise to inform and ensure timely delivery of trial enrollment and quality data

  • Development of strategic institutional/site relationships to optimize the delivery of clinical trial programs; including across therapeutic areas where applicable

Clinical Trial Management

  • Responsible for the development and implementation of applicable site risk plans to ensure delivery of clinical trial enrollment commitments and database locks

  • Ensure site and country level inspection readiness at all times

  • Leverage metrics to inform site/country/regional level decision making

  • Work with internal and external teams to remove barriers to trial execution at a site and/or country level

  • Responsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as required

  • Provide vendor oversight for site monitoring activities at site/country level

Business Management and Engagement

  • Establishes and develops strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities and provide an unparalleled experience for participation in Lilly clinical trials.

  • Cross functional collaboration and partnership to ensure alignment in priorities and deliver the portfolio

  • Perform targeted sites prospecting in alignment with portfolio strategy & priority

  • Maintain therapeutic and technical expertise to enable scientific discussions with the investigator and site personnel

  • Serve as an effective communication “bridge” between sites, third party vendors and Lilly

  • Influence and challenge internal and external factors in order to improve clinical research delivery

Basic Qualification Requirements:

  • Bachelor’s degree or equivalent in a scientific or health-related field

  • Minimum of 3 years experience in the pharmaceutical industry and/or clinical research

  • Valid driver’s license and acceptable driving record

Additional Preferences:

Therapeutic experience in Type 1 or Type 2 diabetes

  • Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs

  • Strong communication (both verbal and written) and language skills

  • Demonstrated exemplary teamwork/interpersonal skills

  • Demonstrated problem solving, attention to detail and result oriented behaviors in a fast-paced environment.

  • Demonstrated leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertainty

  • Strong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as needed

  • Demonstrated ability to enhance/improve customer experience

  • Strong knowledge in country regulatory guidelines/requirements

  • Demonstrated decision-making ability

  • Ability to develop and apply creative solutions

Additional Information:

  • Travel required (50-75%)

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.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

#WeAreLilly

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