SR: TRial Capabilities Assiciate

Eli Lilly and Company; Buenos Aires; Presencial; USD 30.000 - 40.000; Jornada completa

Descripción de la vacante

A global healthcare leader is seeking a Trial Capabilities Associate in Buenos Aires. This role involves supporting clinical trial operations, ensuring investigator site compliance, and managing trial documentation. Candidates should have a Bachelor's degree in a related field and at least two years of experience in clinical research. Strong organizational and communication skills are essential for success in this position.

Formación

• 2 years of clinical research experience in start-up/regulatory area.
• Understanding of clinical development and site activation.
• Knowledge of project management processes.

Responsabilidades

• Ensure investigator sites meet requirements for clinical trials.
• Manage authorizations, budget execution, and contract activities.
• Maintain a complete and accurate Trial Master file.

Conocimientos

Effective communication

Negotiation skills

Problem solving

Self-management

Organizational skills

Educación

Bachelor´s degree in a scientific or health-related field

Descripción del empleo

SR: TRial Capabilities Assiciate page is loaded

SR: TRial Capabilities Assiciate

Apply locations Argentina, Buenos Aires time type Full time posted on Posted Yesterday job requisition id R-90668

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 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 clinical finance, record management and site training. The associate will ensure inspection readiness though a complete, accurate and readily available Trial Master file. Additional local responsabilities 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 of clinical research experience (start-up/regulatory area)
• 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 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 ( https://careers.lilly.com/us/en/workplace-accommodation ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lillydoes 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

About Us

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!