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Clinical Development Consultant

hace 4 meses

Buenos Aires, Argentina Lilly A tiempo completo
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 35,000 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.


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 timely delivery of clinical trial enrollment in accordance with scientific objectives, timely 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, leveraging of information/tools to make/have informed decisions and discussions, and high quality interactions with global clinical trial sites to drive to an unparalled 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 Responsabilities

Clinical Investigator Management

  • Accountable for 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
  • Accountable for comprehensive site management activities to ensure timely delivery of enrollment readiness, trial recruitment/enrollment and database locks; inclusive of performance management and issue mitigation, identification and resolution
  • Responsible for identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience
  • Accountable for the development of strategic institutional/site relationships to optimize the delivery of clinical trial programs; including across therapeutic areas where applicable
  • Clinical Trial Managment
  • 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
Minimum 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 and strong working knowledge of Good Clinical Practice
  • Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs
  • Strong selfmanagement and organizational skills; ability to manage workload, set personal priorities and adjust as needed
Additional Preferences

Strong communication (both verbal and written) and language skills

  • Strong organisational/planning skills
  • Demonstrated ability to enhance/improve customer experience
  • Fluent in English as well as required language to conduct daytoday business
  • Strong knowledge in country regulatory guidelines/requirements
  • Strong teamwork and interpersonal skills
  • Demonstrated decisionmaking ability
  • Demonstrated strategic agility &