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.
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