Empleos actuales relacionados con Trial Capabilities Associate - Buenos Aires - Eli Lilly
-
Trial Capabilities Associate
hace 1 semana
Buenos Aires, Argentina Eli Lilly A tiempo completoAt 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...
-
Sr: Trial Capabilities Assiciate
hace 22 horas
Capital Federal, Buenos Aires, Argentina Emprego AR A tiempo completo**Detalles de la oferta**: 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...
-
Trial Capabilities Assistant
hace 6 días
Buenos Aires, Argentina Lilly A tiempo completoAt 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...
-
Local Trial Manager
hace 1 semana
Buenos Aires, Argentina IQVIA A tiempo completoLocal Trial Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in the country. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial team is...
-
Clinical Trial Assistant
hace 22 horas
Buenos Aires, Argentina IQVIA A tiempo completo**Join us as a **Clinical Trials Assistant!**: **What You´ll Do** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...
-
Clinical Trial Assistant
hace 22 horas
Buenos Aires, Argentina IQVIA A tiempo completo**Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...
-
Clinical Trial Project Manager
hace 1 semana
Buenos Aires, Argentina Medpace A tiempo completoJob Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Buenos Aires, Argentina . Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS, and more. We offer a very competitive...
-
Senior Clinical Associate
hace 4 días
Buenos Aires, Argentina Icon plc A tiempo completoSenior Clinical Associate - Buenos Aires, Argentina ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of...
-
Clinical Trial Manager
hace 2 semanas
Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completoClinical Trial Manager – Sponsor Dedicated.Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at country level for end-to-end project management from start-up through to closeout activities.Tasks & Responsibilities: • Services...
-
Clinical Trial Project Manager
hace 1 semana
Buenos Aires, Buenos Aires C.F., Argentina Medpace, Inc. A tiempo completoMedpace is the leading CRO for Biotech companies and is continuing to add and established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Buenos Aires, Argentina. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We offer a very competitive salary/bonus...
Trial Capabilities Associate
hace 2 semanas
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 Trial Capabilities Associate provides clinical trial capabilities in support of clinical development. The associate is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing activities during site maintenance and close-out. The associate is responsible for obtaining clinical trial authorizations and ethical approvals, execution of the budget and contract, and activities related to clincial finance, records management and site training. The associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File. Additional local responsibilities may be required as needed/appropriate for the local geography and/or to cover regional differences.
- Minimum Qualifications requirements:
- Bachelor’s degree preferably in a scientific or health related field, two years clinical research experience or relevant experience preferred
- . Understanding of the overall clinical development paradigm and the importance of efficient site activation
- Applied knowledge of project management processes and skills
- Appreciation of / experience in compliance-driven environment
- . Ability to learn and comply with financial and legal guidelines and policies (budget and contract)
- Effective communication, negotiation, and problem solving skills
- Self-management and organizational skills
- Language Capabilities
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