Clinical Research Lead

Há 1 mês

São Paulo, Brasil Eli Lilly and Company Tempo inteiro

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.

The Clinical Research Lead (CRL) is responsible for the management of clinical Investigators and sites being considered and/or participating in Lilly clinical trials.

CRLs are broadly responsible for the performance at site and country level, inclusive of Investigator/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.

The CRL is also responsible for oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.

Primary Responsibilities

  1. 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.
  2. Accountable for comprehensive investigator 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.
  3. Responsible for identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience.
  4. Accountable for the application of scientific, therapeutic area, and institutional/regional expertise to inform and ensure timely delivery of trial enrollment and quality data.
  5. Accountable for the development of strategic institutional/site relationships to optimize the delivery of clinical trial programs; including across therapeutic areas where applicable.
  6. Responsible for the development and implementation of applicable investigator/site risk plans to ensure delivery of clinical trial enrollment commitments and database locks.
  7. Ensure site and country level inspection readiness at all times.
  8. Leverage metrics to inform site/country/regional level decision making.
  9. Work with internal and external teams to remove barriers to trial execution at a site and/or country level.
  10. Responsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as required.
  11. Provide vendor oversight for site monitoring activities at site/country level.
  12. Establish and develop 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.
  13. Cross-functional collaboration and partnership to ensure alignment in priorities and deliver the portfolio.
  14. Perform targeted sites prospecting in alignment with portfolio strategy & priority.
  15. Maintain therapeutic and technical expertise to enable scientific discussions with the investigator and site personnel.
  16. Serve as an effective communication “bridge” between sites, third party vendors and Lilly.
  17. Influence and challenge internal and external factors in order to improve clinical research delivery.

Qualifications Requirements for this position:

  1. Bachelor’s degree or equivalent.
  2. Minimum of 4 years experience in the pharmaceutical industry and/or clinical research. Preference for working knowledge of Good Clinical Practice.
  3. Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs.
  4. Strong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as needed.
  5. Demonstrated strategic agility & broad business acumen.
  6. Demonstrated leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertainty.
  7. Strong communications skills, and ability to influence others.
  8. Fluent in English and Portuguese.

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.

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

#J-18808-Ljbffr

  • Senior Clinical Research Lead

    Há 8 horas

    São Paulo, São Paulo, Brasil Cti Clinical Trial Services, Inc Tempo inteiro

    About CTI Clinical Trial Services, IncCTI Clinical Trial Services, Inc is a leading contract research organization (CRO) dedicated to advancing medicine through clinical trials. Our team of experts works tirelessly to ensure the highest quality results and exceptional patient care.We value our employees as the backbone of our success, providing a supportive...

  • Clinical Research Operations Lead

    3 semanas atrás

    São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    At ICON Plc, we are a world-leading healthcare intelligence and clinical research organisation dedicated to advancing clinical research.We provide outsourced services to pharmaceutical, biotechnology, medical device, and government organisations, accelerating the development of drugs and devices that save lives and improve quality of life.Our people are at...

  • Clinical Research Professional

    4 semanas atrás

    São Paulo, São Paulo, Brasil Novasyte Tempo inteiro

    Key Responsibilities:We are seeking a skilled Clinical Research Professional to provide clinical research support to investigators and site staff. Key responsibilities include verifying and/or correcting research study information on source documents, responding to research queries and variances, and providing feedback to the site data collector.The ideal...

  • Clinical Research Coordinator

    1 semana atrás

    São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    At ICON plc, a world-leading healthcare intelligence and clinical research organization, we're proud to foster an inclusive environment driving innovation and excellence. Our mission is to shape the future of clinical development, and we're seeking a skilled Clinical Trial Administrator to join our diverse and dynamic team.We offer a competitive salary range...

  • Clinical Research Associate

    Há 3 dias

    Sao Paulo, Brasil Medpace, Inc. Tempo inteiro

    Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an **exciting career** in the research of drug and medical device development. For those with **medical and/or health/life science interest and background** who want to explore the research field, **travel throughout Brazil**, and be part of a team bringing...

  • Principal Clinical Research Associate

    7 meses atrás

    Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    **Principal Clinical Research Associate** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or...

  • Senior Clinical Research Specialist

    3 semanas atrás

    São Paulo, São Paulo, Brasil Icon Tempo inteiro

    Job Title: Senior Clinical Research SpecialistAbout the Company:ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical...

  • Clinical Research Associate

    3 semanas atrás

    São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    About ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We advance clinical research by providing outsourced services to pharmaceutical,...

  • Clinical Research Associate

    7 meses atrás

    Sao Paulo, Brasil AbbVie Tempo inteiro

    **Company Description** Describe the primary goals, objectives or functions or outputs of this position. To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves studyrelated clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol...

  • Clinical Research Associate Specialist for Oncology Trials

    3 semanas atrás

    São Paulo, São Paulo, Brasil Parexel International Tempo inteiro

    About the RoleWe are seeking an experienced Clinical Research Associate II to conduct onsite monitoring visits in Brazil. This role offers the opportunity to build and maintain site relationships, ensuring they're set up for success.Key ResponsibilitiesLeverage your expertise to conduct qualification visits, site initiation visits, monitoring visits, and...

  • Clinical Team Lead

    2 semanas atrás

    São Paulo, Brasil Fortrea Tempo inteiro

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology solutions across more than 20 therapeutic areas. With over 18,000 staff conducting...

  • Clinical Research Associate II

    4 semanas atrás

    São Paulo, Brasil Parexel International Tempo inteiro

    In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil. Oncology experience is required. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRAs are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up...

  • Clinical Research Associate II

    3 semanas atrás

    São Paulo, Brasil Parexel International Tempo inteiro

    In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil. Oncology experience is required. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set...

  • Clinical Trials Operations Lead

    3 semanas atrás

    São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro

    At Icon Plc, we're dedicated to advancing clinical research and improving patient outcomes. As a Clinical Trial Manager in our Real World Solutions team, you'll play a critical role in delivering high-quality clinical trials.**Job Summary:**We're seeking an experienced Clinical Trial Manager to oversee the operational aspects of our clinical trials. In this...

  • Clinical Project Manager

    Há 6 dias

    Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    **Clinical Project Manager** **(Level Depends on Experience)** **Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...

  • Health Economics

    7 meses atrás

    Sao Paulo, Brasil Boston Scientific Corporation Tempo inteiro

    **Health Economics & Clinical Research Specialist**: - Remote Eligible: Hybrid- Onsite Location(s): São Paulo, SP, SP, BR**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams...

  • Clinical Research Associate Sr

    Há 2 dias

    Sao Paulo, Brasil MSD Tempo inteiro

    Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine **Main Responsabilities**: Develops strong site relationships and ensures...

  • Clinical Research Associate I

    3 semanas atrás

    São Paulo, São Paulo, Brasil Fortrea Tempo inteiro

    Company OverviewFortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.We...

  • Associate Clinical Research Manager

    9 meses atrás

    Sao Paulo, Brasil Fortrea Tempo inteiro

    The Ass CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...

  • Clinical Research Associate Ii

    Há 4 dias

    Sao Paulo, Brasil PSI CRO Tempo inteiro

    Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate II at PSI...